The IPIC 2015 Organising Committee is glad to announce that 157 abstracts have been approved for poster presentation!

The deadline for submission of abstracts was 30th of June 2015.

The 3 winning abstracts submitters who will be presented with an award and have the opportunity to present their posters in a dedicated session are:

1 – LOSS-OF-FUNCTION MUTATIONS IN IFIH1 PREDISPOSE TO SEVERE VIRAL RESPIRATORY INFECTIONS IN CHILDREN
S. Asgari (1), LJ. Schlapbach (2), S. Anchisi (3), C. Hammer (1), I. Bartha (1), PJ. McLaren (1), T. Junier (1), D. Garcin (3), J. Fellay (1)
2 – A CROSS SECTIONAL STUDY OF GASTROINTESTINAL SYMPTOMS AND PATHOLOGY IN PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY
S. Jørgensen (1), H Reims (3), D Frydenlund (3), K Holm (1,4), V Paulsen (5), A.E. Michelsen (1), K Jørgensen (4), L.T. Osnes (6), J Bratlie (1), T.J. Eide (3), E Holter (7), R Rose (8,9), K Hanevik (8), H-R Brattbakk (8,10), T Fiskåstrand (8,10), T Ueland (1), T.H. Karlsen (1,4), P Aukrust (1,2), K.E.A Lundin (5), B Fevang (1,2)
3 – NEWBORN SCREENING FOR SEVERE PRIMARY IMMUNODEFICIENCIES: IMPACT OF GESTATIONAL AGE AND BIRTH WEIGHT ON T-CELL-RECEPTOR-EXCISION CIRCLES (TRECS) AND KAPPA-DELETING-RECOMBINATION-EXCISION CIRCLES (KRECS
O. Neth (1), B. de Felipe (1), B. Sanchez (1), C. Delgado (1), LM. Lucena (1), A. Pavon (1), J. Casanova (2), C. Salamanca (3), S. Borte (4), P. Olbrich (1)
All approved abstracts:
A 13 YEAR OLD PATIENT WITH GENERALIZED SEIZURES AND HYPOCALCAEMIA – DELAYED DIAGNOSIS OF DIGEORGE SYNDROME
G. Petkovic (1), J. Kelecic (2)
A CASE OF COMBINED IMMUNODEFICIENCY ASSOCIATED TO IMMUNE DYSREGULATION AND THROMBOCYTOPENIA
F. romano (1), S. ricci (2), C. canessa (3), F. lippi (4), L. bianchi (5), R. cupone (6), c. Azzari (7)
A CASE OF SEVERE  CONGENITAL AGAMMAGLOBULINAEMIA WITH PYODERMA GANGRENOSUM AND ARTHRITIS
K. Linauskiene (1), N. Buterleviciute (1,2,3), A. Blaziene (1,2)
A CLINICAL AND LABORATORY PROFILE OF CHRONIC GRANULOMATOUS DISEASE DUE TO NCF2 GENE MUTATIONS: OUR EXPERIENCE AT CHANDIGARH, NORTH INDIA
A. Rawat (1), V Pandiarajan (1), D Suri (1), A Gupta (1), B Saikia (2), R Minz (2), KW Chan (3), YL Lau (3), S Singh (1)
A CROSS SECTIONAL STUDY OF GASTROINTESTINAL SYMPTOMS AND PATHOLOGY IN PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY
S. Jørgensen (1), H Reims (3), D Frydenlund (3), K Holm (1,4), V Paulsen (5), A.E. Michelsen (1), K Jørgensen (4), L.T. Osnes (6), J Bratlie (1), T.J. Eide (3), E Holter (7), R Rose (8,9), K Hanevik (8), H-R Brattbakk (8,10), T Fiskåstrand (8,10), T Ueland (1), T.H. Karlsen (1,4), P Aukrust (1,2), K.E.A Lundin (5), B Fevang (1,2)
A FAMILY  WITH  WISKOTT -ALDRICH – LIKE  SYNDROME DUE TO MUTATION IN THE WIP  F1 GENE
M. albahkali (1), R Arnaout (2), M Dasouki (3), H Al-Dhekri (4), H Al-Mousa (5), A Al-Ghonaium (6), B alsaud (7), S almohsen (8), S Al-Hiss (9), L Al Baik (10)
A LATE ONSET CHEDIAK-HIGASHI SYNDROME IN A 16 YEAR OLD GIRL, WITHOUT SILVERY HAIR AND OCULOCUTANEOUS ALBINISM
M. Fazlollahi (1), S. Khandan Alamdari (1), A. Hamidieh (2), Z. Pourpak (1)
A NEW IL-2RG GENE MUTATION IN AN X-LINKED SCID IDENTIFIED THROUGH TREC/KREC SCREENING: A CASE REPORT
M. Nourizadeh (1), S. Borte (2,3), MR. Fazlollahi (1), L. Hammarström (2), Z. Pourpak (1)
A NEW STAT3 MUTATION IN A FAMILY WITH A PRIMARY ANTIBODY DEFICIENCY
N. Suratannon (1), S. Swagemakers (3,4), W. Dik (2), E. van de Vosse (5), M. van der Burg (2), V. Dalm (2), P. J. van der Spek (3), M. Wentink (2), G J. Driessen (6), PM van Hagen (1.2.7)
A NOVEL CYBB MUTATION IN AN IRANIAN BOY WITH CHRONIC GRANULOMATOUS DISEASE
S. Tajik (1), M.R. Fazlollahi (1), M. Badalzadeh (1), M. Houshmand (2), F. Zandieh (3), S. Khandan alamdari (1), Z. Pourpak (1)
A NOVEL HETEROZYGOUS C.1957G>A (P.(VAL653ILE)) MUTATION OF STAT1 IN A FAMILY CAUSING CHRONIC MUCOCUTANEOUS CANDIDIASIS AND AUTOIMMUNITY
K. Meesilpavikkai (1), W.A. Dik (1), P.M. van Hagen (1, 2), G.J.A. Driessen (1, 3), V.A.S.H. Dalm (1, 2)
A NOVEL MUTATION IN DOCK8 AR-HIGE SYNDROME IN ONE FAMILY ASSOCIATED WITH SEVERE PHONOTYPE AND SUCCESSFUL HEMATOPIETIC STEM CELL TRANSPLANTATION
L. Alshekaili (1), S. Al Gazlan (2), H Al Dhekri (3), H. Al Mousa (4), F. Sheikh (5), A. Al Ghonaim (6), B. Al Saud (7), S. Al Muhsen (8), K. Rehan (9), S. Al Sumayli (10), M. Al Zahrani (11), A. Dababo (12), A. Al Qawi (13), F. Al Ahmadi (14), A. Hawwari (15), R. Arnaout
A NURSE’S EXPERIENCE OF A COMPANY-SPONSORED PATIENT SUPPORT PROGRAM FOR HOME SUBSTITUTIVE TREATMENT OF IMMUNODEFICIENT PATIENTS WITH SUBCUTANEOUS POLYVALENT IMMUNOGLOBULINS
A. Reniers (1)
A POSSIBLE TYPE II BARE LYMPHOCYTE SYNDROME: A CASE REPORT
G. Salgado-Cecilia (1), E. Novoa Bolivar (1), J. Eguia (1), M.R. Moya-Quiles (1), S. Alfayate (2), A. Menasalvas (2), A. Bernal (1), H. Martinez-Banaclocha (1), V. Martinez-Sanchez (1), J.M. Bolarin (1), M. Muro (1), A. Minguela (1), A.M. Garcia-Alonso (1)
A TRIAL OF RAPAMYCIN IN A GIRL WITH PIK3R1 IMMUNODEFICIENCY
E. Valencic (1), V. Lougaris (2), F. Faletra (1), G. Lanzi (2), D. Vozzi (1), A. Marcuzzi (1), E. Piscianz (1), A.M. Bianco (1), M. Girardelli (1), C. Loganes (3), D. Moratto (2), S. Giliani (2), A. Tommasini (1)
ADENOSINE DEAMINASE DEFICIENCY: GENOTYPE-PHENOTYPE CORRELATIONS BASED ON TOXIC METABOLITE LEVELS MEASURED BY TANDEM MASS SPECTROMETRY
F. romano (1), c. Canessa (2), F. Lippi (3), S. Ricci (4), R. Cupone (5), G. La Marca (6), C. Azzari (7)
AN ANALYSIS OF RESPIRATORY TRACT EXACERBATIONS IN PATIENTS WITH CVID
J Sperlich (1, 3), JR Hurst (1, 2), S Workman (1), B Grimbacher (1, 3), DM Lowe (1, 2)
AN AUDIT ESTABLISHING THE NEED FOR PSYCHOLOGY WITHIN A SPECIALIST IMMUNOLOGY SERVICE.
M. Campbell (1), A Symes (1), S Workman (1), D Lowe (1)
AN OCCURENCE OF BRONCHIAL ASTHMA AND CHRONIC OBSTRUCTIVE PULMONARY DISEASE IN PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY
T. Milota (1), T. Svobodova (2), R. Zachova (1), E. Vernerova (1), A. Sediva (1)
ASYMPTOMATIC ADULT PATIENT WITH COMPLEMENT FACTOR I DEFICIENCY
I. MAGRIZ TASCON (1), Eyad Madany (1), Carmen Cámara Hijón (1), Jose Antonio García Trujillo (1), Silvia Romero Chala (1), Luis Fernández Pereira (1)
ATYPICAL SCID DUE TO A NOVEL RAG1 MUTATION DIAGNOSED AT THE AGE OF 23 MONTHS
S. Tantou (1), N. Sirimi (2), A. Michos (2), J. Chou (3), M. Tzanoudaki (1), M. Massaad (3), E Lykopoulou (2), R. Geha (3), M. Kanariou (1)
ATYPICAL WISKOTT ALDRICH SYNDROME ASSOCIATED WITH A HETEROZYGOUS MEFV VARIANT PRESENTING WITH AN AUTOINFLAMMATORY PHENOTYPE.
F. Ladomenou (1), K. Brunner (2), M Bajaj-Elliott. (2), P Brogan (3), P Amrolia (4), A Thrasher (1), L Chenchara (1), A Worth (1)
AUTOIMMUNE COMPLICATIONS IN PATIENT WITH ATAXIA TELEANGIECTASIA
V. Urdova (1), M. Gresikova (2), H. Vargova (3), P. Ciznar (1)
BTK GENE MUTATIONS IN PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA
Z. Alizadeh (1), P. Dashti (1), S. Tajik (1), Z. Chavoshadeh (2), M. Movahedi (3), M.R. Fazlollahi (1), Z. Pourpak (1)
CHARACTERIZATION AND ROLE OF INDIRECTLY-ACTIVATED HUMAN DENDRITIC CELLS BY IMMUNE-COMPLEXED ADENOVIRUS IN IMMUNE RESPONSE
T. TRAN (1), K. EICHHOLZ, (1), F. J. D MENNECHET (1), E. J KREMER (1)
CHRONIC GRANULOMATOUS DISEASE AND MCLEOD NEUROACANTHOCYTOSIS SYNDROME: A CONTIGUOUS GENE SYNDROME
E. Novoa Bolivar (1), J. Eguia (1), G. Salgado-Cecilia (1), M.R. Moya-Quiles (1), S. Alfayate (2), A.I. Menasalvas (2), C. Funes (3), A. Bernal (1), J.M. Bolarin (1), M. Muro (1), A. Minguela (1), A.M. Garcia-Alonso (1)
CLINICAL AND GENETIC CHARACTERISTICS OF NINE  UKRAINIAN  PATIENTS WITH  WISKOTT–ALDRICH SYNDROME.
Y. Romanyshyn (1), L. Kostyuchenko (1), L. Marodi (2)
CLINICAL AND IMMUNOLOGICAL CHARACTERISTICS OF 29 SERBIAN PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY
R. Mijanovic (1), B. Bonaci-Nikolic, S. Andrejevic, V. Perovic (2), N. Kraguljac-Kurtovic (3)
CLINICAL CHARACTERIZATION AND TREATMENT OF PATIENTS WITH COMMON VARIABLE IMMUNE DEFICIENCY-SINGLE CENTER EXPERIENCE
E. Naumova Jordanova (1), S. Mihailova (1), N. Gesheva (1), S. Lesichkova (1), M. Baleva (1), A. Temelkov (2)
CLINICAL MANIFESTATIONS AND LABORATORY FEATURES OF MENDELIAN SUSCEPTIBILITY TO MYCOBACTERIAL DISEASE (MSMD) CASES DIAGNOSED AT CHANDIGARH
A. Rawat (1), D Suri (1), A Gupta (1), J Bustamante (2), S Boisson-Dupuis (2), J Casanova (2), K Imai (3), O Ohara (4), S Singh (1)
CLINICAL PRESENTATION AND OUTCOME OF ADULT-ONSET IMMUNODEFICIENCY CAUSED BY ANTI-INTERFERON-GAMMA-AUTOANTIBODIES: A CASE SERIES OF 10 PATIENTS
T. Kampitak (1), K. Jutivorakool (1), C Suankratay (1)
CLINICAL SPECTRUM OF PRIMARY IMMUNODEFICIENCIES IN MOROCCO
L. Jeddane (1), H. Ouair (2), Z. Aadam (2), I. Benhsaien (1), A.A. Bousfiha (1), F. Ailal (1)
COMBINED GENETIC DISORDERS IN PRIMARY IMMUNODEFICIENT PATIENTS
V. Mammadova (1), G. Nasrullayeva (1)
COMBINED IMMUNODEFICIENCIES: DISTINCTIVE FEATURES IN MOROCCO
N. RADA (1), L JEDDANE (2), I BENHSSEINE (3), F AILAL (4), J NAJIB (5), AA BOUSFIHA (6)
COMBINED IMMUNODEFICIENCY , SELECTIVE IGM DEFICIENCY & ELEVATED SERUM IGE WITH MYCOBACTERIA INFECTION IN A MALAY CHILD. AN AUTOSOMAL RECESSIVE HYPER-IGE SYNDROME?
A. Ali (1), F. Bakon (3), B. AAziz (1), A. AWahab (2), AH. Abdul Latiff (4), L. MNoh (1)
COMBINED IMMUNODEFICIENCY IN THE UNITED STATES AND KUWAIT: COMPARISON OF PATIENTS’ CHARACTERISTICS AND MOLECULAR DIAGNOSIS
W. Al-Herz (1), L. Notarangelo (2), A. Sadek (3), R Buckley (4), USIDNET Consortium
COMMON VARIABLE IMMUNODEFICIENCY (CVID) PATIENT PRESENTED AS AUTOIMMUNE CITOPENIAS AND SPLENOMEGALY
M. Batnozic Varga (1), J. Kelecic (2), S. Izakovic (1), S. Puseljic (1), M. Arambasic (1)
COMMON VARIABLE IMMUNODEFICIENCY (CVID) TURNED OUT TO BE AN INTESTINAL LYMPHANGIECTASIA. CASE HISTORY.
I. Martynova (1), E. Latysheva (1), T. Latysheva (1)
COMMON VARIABLE IMMUNODEFICIENCY IN 6 ADULT PATIENTS: A TERTIARY CARE CENTRE EXPERIENCE IN NORTH INDIA
D. Sharma (1), A. Rawat, D. Suri, A. Gupta, S. Singh
COMPLEMENT DEFICIENCIES DURING PURULENT MENINGITIS
A. OULADLAHSEN (1)
CONFIRMATION OF HYPER IMMUNOGLOBULIN E SYNDROME IN TWO PATIENTS WITH OCULAR PROBLEM: DETECTION OF TWO NEW DEDICATOR OF CYTOKINESIS 8 MUTATIONS
S. Saghafi (1), F. Zandieh (2), M.R. Fazlollahi (1), S.A. Sarrafzadeh (1), C. Glocker (3), N. Frede (3), M. Buchta (3), L. Yang (3), A.H. Mahmoudi (4), M. Houshmand (5), Z. Pourpak (1/6), B. Grimbacher (3), M. Moin (1/6)
CONGENITAL AGAMMAGLOBULINEMIA IN 87 IRANINA PATIENTS
A. Aghamohammadi (1), H Abolhassani1, M Vitali, V Lougaris, S Giliani, L Parvaneh, A Plebani3
CONGENITAL AGAMMAGLOBULINEMIAS: EXPERIENCE FROM A LEVEL THREE HOSPITAL IN CROATIA
N. Cigrovski (1), D. Tjesic-Drinkovic (1), D. Richter (1), D. Caleta (1), A. Merkler (2), J. Sertic (2), J. Kelecic (1)
CORD BLOOD TRANSPLANTATION WITHOUT T CELL DEPLETION FOR INFANTS WITH MHC CLASS II DEFICIENCY
R. Elfeky (1), J silva (1), R Chiesa (1), K Rao (1), P Amrolia (2), B Gaspar (2), A Worth (1), G Lucchini (1), A Jones (1), L Young (1), S Bibi (3), W Qasim (2), P Veys (1)
CYTOPENIAS IN COMMON VARIABLE IMMUNODEFICIENCY (CVID)
M. Carrabba (1), R.M. Dellepiane (2,3), L. Dell’Era (2,3), C. Caccia Dominioni (2,3), M.C. Pietrogrande (2,3), G. Fabio (1,3)
DATA FROM PRIMARY IMMUNODEFICIENCY CENTRE OF THE HOSPITAL OF LITHUANIAN UNIVERSITY OF HEALTH SCIENCES IN THE CONTEXT OF EUROPEAN REGISTRY FOR PRIMARY IMMUNODEFICIENCIES
L. Tamasauskiene (1), I. Bajoriuniene, B. Sitkauskiene
DETECTION OF COMPLICATIONS FOLLOWING INTRAVENOUS IMMUNOGLOBULINS INFUSION IN A COHORT OF EGYPTIAN CHILDREN
A. Elmarsafy (1), N. Galal (1), S. Abdallah (1), I. Youssry (1)
DIAGNOSIS OF IRANIAN MENDELIAN SUSCEPTIBLITY TO MYCOBACTERIAL DISEASES PATIENTS IN A PROLIFERATION AND CYTTOKINE PRODUCTION
S. Sarrafzadeh (1), M Mahloujirad (1), M Nourizadeh (1), M Fazlollahi (1), z Pourpak (1), M Moin (1)
DIGEORGE/CHROMOSOME 22Q11.2 DELETION SYNDROME: CLINICAL AND IMMUNOLOGICAL FINDINGS IN 23 PATIENTS FROM THE GROUP OF PRIMARY IMMUNODEFICIENCIES IN MEDELLÍN, COLOMBIA
E. Vasquez (1), C. Trujillo-Vargas, J. Orrego-Arango, J Franco-Restrepo
DISEASE-TARGETED SEQUENCING: A POTENT NEXT-GENERATION SEQUENCING APPROACH SUCCESSFULLY EMPLOYED TO IDENTIFY DISEASE CAUSING MUTATIONS IN PRIMARY IMMUNODEFICIENCIES (PIDS)
A. Krolo (1), T. Hirschmugl (1), I. Bilic (1), B. Erman (2), J. Arora (1), M. Schuster (1), K. Boztug (1,3)
DISSEMINATED MYCOBACTERIUM KANSASII AND BACILLUS CALMETTE-GUERIN RELATED IMMUNE RECONSTITUTION INFLAMMATORY SYNDROME IN HAPLOIDENTICAL STEM CELL TRANSPLANT IN SEVERE COMBINED IMMUNODEFICIENCY INFANT
V. RAJENDRAN (1), TJ. MOHAMED (1), KA MOHD RAZALI (1), IS OTHMAN (1), IH ISMAIL (2)
DIVERSE CLINICAL PHENOTYPES IN RECOMBINASE-ACTIVATING GENE 1 DEFICIENCY
N. Karaca (1), G. Aksu (1), E. Ulusoy (1), N. Kutukculer (1)
DOSING SCHEDULES FOR INITIATION AND MAINTENANCE THERAPY WITH 20% SUBCUTANEOUS IMMUNOGLOBULIN (HIZENTRA) IN PRIMARY IMMUNODEFICIENCY
A. Hubsch (1), J. Sidhu (2), M. Rojavin (3)
ECTODERMAL DYSPLASIA WITH IMMUNODEFICIENCY (EDA-ID)
D. Cabanillas (1), P. Del Palacio (1), A. Bernasconi (2), J. Rossi (2), J. Yancoski (2), V. Goris (2), L. Regairaz (1)
EFFECTIVE USE OF 20% SUBCUTANEOUS IMMUNOGLOBULIN THERAPY IN AN ADULT MALE WITH PRE-EXISTING THROMBI
C. Duff (1), M Sher (1), J W Leiding (1)
EFFICACY, PHARMACOKINETICS AND SAFETY OF IQYMUNE®, A NOVEL 10% INTRAVENOUS IMMUNOGLOBULIN IN PATIENTS WITH PRIMARY IMMUNE DEFICIENCY: AN OPEN-LABEL MULTICENTRE STUDY
G Krivan (1), L Chernyshova (2), L Kostyuchenko (3), A Lange (4), Z Nuyl (5), B Derfalvi (6), J Musial (7), A Bellon (8), M Kappler (9), A Sadoun (8), E Bernatowska (10)
EFFICACY, SAFETY, AND TOLERABILITY OF HUMAN IMMUNE GLOBULIN SUBCUTANEOUS, 20%: INTERIM ANALYSIS OF A PHASE 2/3 STUDY IN PATIENTS WITH PRIMARY IMMUNODEFICIENCIES IN NORTH AMERICA
D. Suez (1), I. Melamed (2), I. Hussain (3), M. Stein (4), S. Gupta (5), K. Paris (6), S. Fritsch (7), B. McCoy (8), L. Yel (9)
EVALUATION OF PHYSICAL DEVELOPMENT IN CHILDREN WITH PRIMARY IMMUNODEFICIENCY
A. Lewandowicz Uszynska (1), K. Pieniawska (2), M. Babicki (2), M. Bar (2), K. Smiech
EVALUATION OF RAPID PUSH AS AN ADDITIONAL METHOD FOR SUBCUTANEOUS SELF-INJECTIONS OF GAMMANORM® AT HOME. PROTOCOL OF THE “GAMEXPRESS” STUDY
Boris Bienvenu (1), Catherine Ollivier (1), Cyrille Hoarau (2), Benjamin Barin (2), Eric Hachulla (3), Sylvie Brice (3), Anne-Laure Fauchais (4), Françoise Renon (4), Jean-François Viallard (5), Stéphanie Tamisier (5), Yves Mataix (6), Dominique Lachaux (6), Laurent Sailler (7), Frédéric Eyvrard (7), Roland Jaussaud (8), Philippe Benoit (8), Aurélie Delayen (9), Jean-Charles Crave (9), Grégoire Cozon (10)
EVAULATION OF THE PATIENTS WHO HAVE CHRONIC GRANULOMATOUS DISEASE: KONYA EXPERIENCE
E. Hazar Sayar (1), S.N. Guner (1), M. Kirac (1), B. Gokturk (2), H. Artaç (3), S. Keles (1), M. Emiroglu (4), B. Saraymen (5), M.Y. Koker (5), I. Reisli (1)
FIRST REPORT OF GENETIC ANALYSIS OF HERMANSKY PUDLAK SYNDROME TYPE2 IN IRAN
Z Alizadeh (1), S Nabilou (2), F Zandieh (3), A.A Hamidieh (4), M.M Fazlollahi (1), Z Pourpak (1)
FMF MAY NOT BE THE REAL CAUSE OF ABDOMINAL ATTACKS IN MEDITERRANEAN PEOPLE: DO NOT MISS HAE!
S. ARSLAN (1), R. UCAR (1), S. SOYYIGIT (1), K. AYAR (2), A. KUCUK (2), R. TUNC (2), AZ. CALISKANER (1)
FROM ENVIRONMENT TO TREATMENT: GIARDIASIS RECALCITRANT TO TREATMENT IN A CVID PATIENT
S. Soyyigit (1), R. UCAR (1), S. ARSLAN (1), S. SAGLAM (2), A.Z. CALISKANER (1)
GENETIC STUDY OF DIFFERENT TYPES OF HIGM PATIENTS
E Bani Jamali (1), Z Aliadeh (1), M.R. Fazlollahi (1), L Atarod (2), Z Pourpak (1)
GUT MICROBIOTA PROFILE IN COMMON VARIABLE IMMUNODEFICIENCY ASSOCIATES WITH SYSTEMIC IMMUNE ACTIVATION.
S. Jørgensen (1), M Trøseid (1,2), M Kummen (1,3), J.A. Anmarkrud (1,3), A.E. Michelsen (1), L.T. Osnes (4), K Holm (1,3), M.L. Høivik (5), A Rashidi (1), C.P. Dahl (1), R.K. Berge (6,7), B Moum (5), K.E.A. Lundin (8), B. Fevang (1,2), T Ueland (1), T.H, Karlsen (1,3,8), P Aukrust (1,2), J.E.R. Hov (1,3,8)
HAEMATOPOIETIC STEM CELL TRANSPLANTATION IN PEDIATRIC PRIMARY IMMUNODEFICIENT PATIENTS IN SLOVAKIA, PROGNOSIS AND OUTCOMES WITHIN YEARS 2001-2015.
P. Ciznar (1), J. Horakova (2), I. Bodova (2), M. Hricova (1), P. Svec (2), S. Sufliarska (2), L. Libai-Vegh (1), J. Chocholova (2), J. Adamcakova (2), D. Tanuskova (2), T. Sykora (2), M. Pozdechova (2), A. Kolenova (2)
HEREDITARY ANGIOEDEMA: A REPORT ON THE DELAYED DIAGNOSIS IN CHILDREN AND ADOLESCENTS
M. Ayazi (1), M.R. Fazlollahi (1), F. Kargarsharif (1), N. Mehranmehr (1), I. Mohammadzadeh (2), M. Nabavi (3), A. Fayezi (4), M. Movahedi (5), S. Saghafi (1), Z. Pourpak (1)
HEREDITARY ANGIOEDEMA: THE POSSIBILITY OF EARLY DETECTION IN CLINICAL HOSPITAL
M. Karakina (1), E. Karbovnichaya (2), D. Mazein (3)
HUMAN DOCK2 MUTATIONS UNDERLIE A NOVEL, PLEIOTROPIC IMMUNODEFICIENCY SYNDROME WITH EARLY ONSET, INVASIVE INFECTIONS
C. DOMINGUEZ CONDE (1), K DOBBS (2), SY ZHANG (3, 4, 5), S PAROLINI (6), M AUDRY (3), E HAAPANIEMI (7), S KELES (2,8), I BILIC (1), MJ MASSAAD (2), TA CHATILA (2), RS GEHA (2), L ABEL (3,4,5), RH BUCKLEY (9), A IKINCIOGULARI (10), W AL-HERZ (11), M HELMINEN (12), F DOGU (10), JL CASANOVA (3,4,5), K BOZTUG (1), LD NOTARANGELO (2)
IDENTIFICATION OF MONOGENIC CAUSES OF CHRONIC EARLY-ONSET DIARRHEA USING NEXT GENERATION SEQUENCING
R. Ardy (1), T. Hirschmugl (1), C. Domínguez Conde (1), N. Serwas (1.), Z. Kuloglu (2), A. Kansu (2), K. Boztug (1, 3)
IMMUNODEFICIENCIES WITH DEFECTS IN PI(3)K FUNCTION IN RUSSIAN CLINICAL CHILDREN’S HOSPITAL, MOSCOW.
I. Kondratenko (1), O. Pashchenko (2), S. Vakhlyarskaya (1), S. Sharapova (3), I. Guryanova (3), M. Belevtsev (3)
IMPAIRMENT OF THE ENDOCRINE AXIS IN PATIENTS WITH PRIMARY ANTIBODY DEFICIENCIES (PAD)
P. Chunharojrith (1), V. A.S.H. Dalm (1, 2), E. C. Coopmans (1), M. W. van der Ent (2), A-J van der Lely (1), M. van der Burg (2), K. van Bilsen (1), P. Martin van Hagen (1, 2), S. J.C.M.M. Neggers (1)
INFECTIONS IN CHRONIC GRANULOMATOUS DISEASE: 22 YEARS’ SINGLE CENTRE EXPERIENCE FROM NORTH INDIA
V. Pandiarajan (1), A. Rawat (1), A. Sharma (1), D. Suri (1), A. Gupta (1), S. Singh (1)
INFLAMMATORY BOWEL DISEASE AFTER HAEMOPOIETIC STEM CELL TRANSPLANTATION FOR CHRONIC GRANULOMATOUS DISEASE
H. Akturk (1), M. Sutcu (1), Z. Hizli (1), S. Cantez (2), S. Hancerli Torun (1), O. Durmaz (2), A. Somer (1), N. Salman (1)
INFORMATIVENESS OF DOMESTIC TEST-SYSTEM FOR NEWBORNS TREC AND KREC SCREENING
M. Bolkov (1), S. Deryabina (1), I. Tuzankina (1), A. Prodeus (2)
INTRAVENOUS  IMMUNOGLOBULINE TREATMENT OF PATIENTS  WITH PRIMARY IMMUNODEFICIENCY DESEASE IN OUR HOSPITAL
M. TESIC (1), S. Zdravkovic (1), G. Ristic (1), G. Petrovic (1), A. Minic (1), S. Pasic (1)
IPEX-LIKE : CLINICAL PRESENTATIONS IN EGYPT
D. Abd Elaziz (1), S Meshaal (2), R Elhawary (2), N Galal (1), R Alkady (1), A Eldash (1), S Lotfy (1), J Boutros (1), A El Marsafy (1)
LONG-TERM SAFETY, EFFICACY, AND TOLERABILITY OF RECOMBINANT HUMAN HYALURONIDASE-FACILITATED SUBCUTANEOUS INFUSION OF IMMUNOGLOBULIN G IN PATIENTS AGED <18 YEARS WITH PRIMARY IMMUNODEFICIENCIES
RL Wasserman (1), I Melamed (2), M Stein (3), L Kobrynski (4), J Puck (5), S Gupta (6), W Engl (7), B McCoy (8), H Leibl (9), L Yel (10)
LONG-TERM SAFETY, EFFICACY, AND TOLERABILITY OF RECOMBINANT HUMAN HYALURONIDASE-FACILITATED SUBCUTANEOUS INFUSION OF IMMUNOGLOBULIN G IN PATIENTS AT LEAST 18 YEARS WITH PRIMARY IMMUNODEFICIENCIES
RL Wasserman (1), M Stein (2), L Kobrynski (3), S Gupta (4), JA Grant (5), A Rubinstein (6), W Engl (7), B McCoy (8), H Leibl (8), L Yel (9)
LOSS-OF-FUNCTION MUTATIONS IN IFIH1 PREDISPOSE TO SEVERE VIRAL RESPIRATORY INFECTIONS IN CHILDREN
S. Asgari (1), LJ. Schlapbach (2), S. Anchisi (3), C. Hammer (1), I. Bartha (1), PJ. McLaren (1), T. Junier (1), D. Garcin (3), J. Fellay (1)
LPS-RESPONSIVE BEIGE-LIKE ANCHOR GENE MUTATION IN A PATIENT WITH BRONCHIOLITIS OBLITERANS ORGANIZING PNEUMONIA ASSOCIATED WITH HYPER IGM PHENOTYPE AND LOW NUMBER OF B CELLS
S. shokri (1), M. nabavi (1), T. hirschmugl (2), A. Aghamohammadi (3), S. arshi (1), MH. bemanian (1), M. fallahpour (1), R. molatefi (1), M. rekabi (1), N. eslami (1), J. ahmadian heris (1), K. darabi (1), GR. sedighi (1), N. parvaneh (3), K. boztug (4), N. rezaei (5)
MANAGEMENT OF ADVERSE EVENTS IN THE TREATMENT OF PATIENTS WITH INTRAVENOUS IMMUNOGLOBULIN THERAPY : A LITERATURE REVIEW.
Patrick Cherin (1), Jacques Dantal (2), Isabelle Marie (3), Eric Pelus (4), Jean-Charles Crave (5), Jean-Christophe Delain (5), Mauricette Michallet (6), Jean-François Viallard (7)
MELANOCORTIN RECEPTOR AGONIST BMS-470539 ATTENUATES LIPOPOLYSACCHARIDE-INDUCED NEUTROPHIL ACTIVATION AND ACUTE LUNG INJURY
S. kwak (1)
MONOZYGOTIC   SUDANESE TWINS WITH SEVERE COMBINED IMMUNE DEFICIENCY
R. Yahia (1), sara abdelsalam (2), nahal erwa (3), fathia abdelmajeed (2)
MUCOCUTANEOUS LEISHMANIASIS IN A GIRL WITH  ATAXIA TELANGIECTASIA
Y. Barrassali Sulaman (1), I. Matoug (2), H. Salheen (3), S. Alamroni (4), F. Tajori (5)
MYTAPIR, MYPOPI MEDICAL EDUCATION CAMPAIGN: A PILOT STUDY ON PRIMARY IMMUNODEFICIENCY DISEASES (PID) AWARENESS AMONG MEDICAL STUDENTS AND NURSES IN SOUTH EAST ASIA
A. Ali (1), S. Lai (2), B. Lim (3), K. Koh (3), F. Bakon (4), AH. AbdulLatiff (5), N. Surathannon (6), L. MNoh (1)
NATURAL KILLER (NK) CELL DEFICIENCY: A THREE-CASE REPORT
Larrauri (1), C. Domaica (3), D. Fernandez Romero (1,2), C. Juri (1,2), G. Torre (1,2), E. Malbran (1,2), N. Zwirner (3), A. Malbran (2)
NEWBORN SCREENING FOR SEVERE COMBINED IMMUNE DEFICIENCY (SCID) IN ONTARIO, CANADA: THE PROCESS OF ADDITION
L. Gallagher (1), B.K. Potter (1,2), C.A. Rupar (4), P. Chakraborty (1,3), C.M. Roifman (5,6,7,8), B. Reid (5,6,8), M.T Geraghty (1,3)
NEWBORN SCREENING FOR SEVERE PRIMARY IMMUNODEFICIENCIES: IMPACT OF GESTATIONAL AGE AND BIRTH WEIGHT ON T-CELL-RECEPTOR-EXCISION CIRCLES (TRECS) AND KAPPA-DELETING-RECOMBINATION-EXCISION CIRCLES (KRECS
O. Neth (1), B. de Felipe (1), B. Sanchez (1), C. Delgado (1), LM. Lucena (1), A. Pavon (1), J. Casanova (2), C. Salamanca (3), S. Borte (4), P. Olbrich (1)
NIJMEGEN BREAKAGE SYNDROME IN UKRAINE: FREQUENCY, MEDICAL SUPPORT AND FOLLOW-UP
L. Kostyuchenko (1), Y. Romanyshyn (1), I. Savchak (1), H. Makukh (2), H. Akopjan (2), N. Markevych (2)
NON-INTERVENTIONAL POST-AUTHORIZATION SAFETY STUDY (PASS) ON THE LONG-TERM SAFETY OF RECOMBINANT HUMAN HYALURONIDASE (RHUPH20)-FACILITATED SUBCUTANEOUS IMMUNOGLOBULIN G (IGHY)
K Fielhauer (1), A Nagy (2), C Hermann (3), N Nikolov (4), L Yel (5)
NON-INTERVENTIONAL POST-MARKETING SAFETY STUDY ON THE LONG-TERM SAFETY OF HYQVIA (GLOBAL)
K Fielhauer (1), A Nagy (2), C Rabbat (3), B McCoy (4), H Leibl (4), L Yel (5)
OUR SUBCUTANEOUS IMMUNOGLOBULIN REPLACEMENT THERAPY EXPERIENCE WITH INTRAVENOUS PREPARATION
Ö. Özdemir (1), D. Bingöl Aydin (2)
OUTCOME ALLOGENIC HEMATOPOIETIC STEM CELL TRANSPLANTATION IN AUTOSOMAL RECESSIVE HYPER-IGE SYNDROME DUE TO DOCK8 DEFICIENCY: SINGLE CENTER EXPERIENCE
S. Elshorbagi (1), R. Arnaout (2), H. Aldhekri (3), H. Almousa (4), A. Alghonaium (5), B. Alsaud (6), S. Almuhsen (7), M Ayes (8), N. Ades (9), G. AlDawsari (10), A. AlAhmari (11), A. AlSeraihi (12), A. Hawwari (13), L. Alshekaili (14)
OUTCOME OF ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION IN AUTOSOMAL RECESSIVE HYPER-IGE SYNDROME DUE TO DOCK8 DEFICIENCY: SINGLE CENTER EXPERIENCE
S. Abdelrahman Elshorbagi (1), R. Arnaout (1), H. Al-Mousa (1), H. Al-Dhekri (1), A. Al-Ghonaium (1), B. Al-Saud (1), S. Al- Muhsen (1), A. Hawwari (1), N Ades (1), M Ayas (1), G. Al-Dawsari (1), A. AlAhmari (1), A. Al-Seraihi (1)
PANHYPOGAMMAGLOBULINEMIA SECONDARY TO RITUXIMAB TREATMENT OF NON-HODGKIN LYMPHOMA: A SERIES OF CASES.
L. Prestes-Carneiro (1), K Jordão de Souza (2), R Sala Ferro (1), P Andreia Martins Carrilho (3), D Moraes Vasconce (4)
PATIENT EXPERIENCES OF FACILITATED SUBCUTANEOUS IMMUNOGLOBULIN TREATMENT (HYQVIA) FOR PID AND SID:  PRELIMINARY DATA FROM THE SIGNS REGISTRY
Maria Fasshauer (1), Michael Borte (1), David Pittrow (2), Ulrich Baumann (3), Michael Hensel (4), Ralf Gold (8), Doerte Huscher (5), Martin Stangel (6), Marcel Reiser (7), Claudia Sommer (9)
PATIENTS WITH AUTOIMMUNE DISEASE SHOULD BE EVALUATED FOR POSSIBLE UNDERLYING PRIMARY IMMUNODEFICIENCY – DATA FROM THE SLOVENIAN PID REGISTRY
S. Blazina (1), G. Markelj (1), A. Koren Jeverica (1), N. Toplak (1), M. Debeljak (2), A. Ihan (3), T. Avcin (1)
PER – A WAY TO ENSURE BETTER INFORMATION IN A QUALITY REGISTER?
P. Wågström (1), S. Hansen (2), J. Björkander (3), L. Billquist (4), N. Brodszki (5), Å. Nilsdotter (6), M. Nilsson (7), S. Nordeman (8), S. Óskarsdóttir (9), A. Fasth (10)
PID ACTIVITIES IN BENIN
M. ALAO (1)
PIDCARE: A NEW SWEDISH NATIONAL QUALITY REGISTER FOR PRIMARY IMMUNE DEFICIENCIES
J. Björkander (1), S Hansen (2), P Wågström (3), L Billquist (4), N Brodszki (5), Å Nilsdotter (6), M Nilsson (1), S Nordeman (4), S Óskarsdóttir (7), A Fasth (7)
PREFERRED TYPES OF TREATMENT AND THE QUALITY OF PID PATIENTS’ AND THEIR FAMILIES’ LIVES – SURVEY RESULTS
B. Prandzioch (1), A. Górecki (1)
PREGNANCY REGISTRY TO COLLECT LONG-TERM SAFETY DATA FROM WOMEN TREATED WITH RECOMBINANT HUMAN HYALURONIDASE-FACILITATED SUBCUTANEOUS IMMUNOGLOBULIN G (IGHY)
I Baumgartner (1), A Nagy (2), C Hermann (3), N Nikolov (4), C Rabbat (5), L Yel (6)
PREVALENCE OF  HEPATITIS C VIRUS, AND HEPATITIS B VIRUS INFECTION AMONG PATIENTS WITH VARIABLE COMMON IMMUNODEFICIENCY IN TRANSYLVANIA.
D. Deleanu (1), V. Feldrihan (1), E. Pirvu (1), A. Mara (1)
PREVALENCE RATE AND CLINICAL MANIFESTATIONS OF HEREDITARY ANGIOEDEMA IN UNTESTED BLOOD RELATIVES OF THE HEREDITARY ANGIOEDEMA PATIENTS IN A TURKISH CITY
O. Ozdemir (1), B. Elmas (1)
PRIMARY IMMUNODEFICIENCY CARE IN INDONESIA
D. Muktiarti (1), N Kurniati (1)
PRIMARY IMMUNODEFICIENCY DISORDERS IN EGYPT, CAIRO UNIVERSITY 5 YEAR EXPERIENCE
N. Galal (1), S. Meshaal (2), R. El Hawary (2), A.. El Dash (2), R. Alkady (1), D. Abd Elaziz (1), S. Lotfy (1), J. Boutros (1), A. Elmarsafy (1)
PRIMARY IMMUNODEFICIENCY DISORDERS IN VENEZUELA: FIRST REPORT FROM THE VENEZUELAN NETWORK OF PRIMARY IMMUNODEFICIENCY (2011-2015)
M. Herrera Maimone (1), V. Quintero, J. Hanna, D. Delgado, J. Torres, J. A. Cova, M. Bouchard, A. Chacon, J.L. Castillo, L. Benarroch
PRIMARY IMMUNODEFICIENCY IN DEVELOPING COUNTRIES: PERSPECTIVE OF INDONESIAN PEDIATRIC INFECTIOUS DISEASE CONSULTANT
N. Dwi Putri (1), D Muktiarti (1)
PRIMARY IMMUNODEFICIENCY IN INFECTION PRONE CHILDREN IN SOUTHERN SWEDEN: OCCURRENCE, CLINICAL CHARACTERISTICS AND IMMUNOLOGICAL FINDINGS
N. Brodszki (1), G Jönsson (2), L Skattum (3), L Truedsson (3)
PROBABLE (?!) IMMUNE DEFICIENCY – WORDS CAN HARM AND LEAD TO OVERTREATMENT IF ARE NOT ARGUMENTED
O. Turcanu (1)
PROFILE OF LEUKOCYTE ADHESION DEFICIENCY AT A TERTIARY CARE CENTRE IN NORTH INDIA
S. Bhattad (1), D. Suri (1), A. Gupta (1), A. Rawat (1), B. Saikia (2), R. Minz (2), S. Singh (1)
PROFILING AUTOANTIBODIES IN COPD USING ANTIGEN MICROARRAY
R. shindi (1), Ian Todd, Lucy fairclough
PROTECTION AGAINST  PALVIZUMAB RESISTANT RSV  WITH IVIG CONTAINING HIGH TITER ANTI RSV NEUTRALIZING ANTIBODIES
J. mond (1), B. Gilbert
RECENT ADVANCES AND CURRENT STATUS OF PRIMARY IMMUNODEFICIENCY DISEASE IN IRAN
A. Aghamohammadi (1), T Shokuhfar, B Torabi Sagvand, H Abolhassani
RECURRENT PNEUMONIA AND ORAL THRUSH IN A 2 YEARS OLD GIRL
L. Kartina (1), N. Permata (2), D Puspitasari (1), Ismoedijanto (1)
RECURRENT UROSEPSIS IN AN ADULT CAUCASIAN MALE
A. Pombinho de Araújo (1), F. Lourenço (1), C. Martins (2), A. Hsu (3), G. Uzel (3), A. Panarra (1), N. Riso (1), M.F. Moraes-Fontes (1)
RECURRENT, MULTIPLE, MULTI ORGAN ASEPTIC ABSCESSESS
K. Darabi (1), S Arshi, M Nabavi, M Bemanian, M Fallahpour, J Ahmadian, S Shokri, N Eslami, R Molatefi, M seddighi
RELATION BETWEEN LYMPHOCYTES AND DENDRITIC CELLS IN PATIENTS SUFFERING FROM COMMON VARIABLE IMMUNODEFICIENCY
E. Grywalska (1), M. Pasiarski (2), A. Grafka (3), A. Bzdek (4), M. Zgurski (1), M. Walankiewicz (1), M. Maj (1), E. Fitas (1), J. Rolinski (1)
REPEATED NIJMEGEN BREAKAGE SYNDROME IN ONE WOMAN AFTER TWO MARRIAGES
S. Sharapova (1), E. Shepelevich, E. Golovataya, I. Guryanova, M. Belevtsev
RESOLUTION OF HYERSPLENISM AND PANCYTOPENIA IN CVID PATIENT AFTER PARTIAL SPLENIC ARTERY EMBOLIZATION: A CASE REPORT AND REVIEW OF LITERATURE
S. Sumayli (1), L Alskekaili, S Algazlan, F Sheikh, H Alrayes, H Aldhekri, A Kkaliq, R Arnaout
RETROSPECTIVE EVALUATION OF 2217 PATIENTS WITH PRIMARY IMMUNODEFICIENCY IN KONYA (TEN-YEAR-EXPERIENCE OF ONE CENTER)
I. REISLI (1), E.H. SAYAR (1), S. GUNER (1), S. KELES (1), H. ARTAC (2), A. YORULMAZ (1), Y. KINALI (1)
SAFETY AND TOLERABILITY OF HUMAN IMMUNOGLOBULIN G, 20%, ADMINISTERED SUBCUTANEOUSLY (IGSC 20%): FINAL ANALYSIS OF A PHASE 2/3 STUDY IN PATIENTS WITH PRIMARY IMMUNODEFICIENCIES IN EUROPE
M. Borte (1), G. Kriván (2), B. Dérfalvi (3), L. Maródi (4), F. Dicso (5), W. Engl (6), B. McCoy (7), H. Leibl (7), L. Yel (8)
SAFETY OF INTRAVENOUS IMMUNOGLOBULIN THERAPY IN PATIENTS WITH PROBABLE ALZHEIMER’S DISEASE: A RANDOMIZED, PLACEBO-CONTROLLED CLINICAL STUDY
D. Gelmont (1), R.G. Thomas (2), J.A. Dyck-Jones (3), S. Fritsch (4), P. Aisen (5), N. Relkin (6)
SCIG FOR PID PATIENTS; SINGLE CENTER MARMARA EXPERIENCE
E. Karakoc-Aydiner (1), A. Kiykim (1), S. Baris (1), E. Nain (1), A. Ozen (1), I. Barlan (1)
SECONDARY AMYLOIDOSIS IN A PATIENT WITH HYPER-IGE SYNDROM
E. MADANY AL-KHEDER (1), L. Fernández Pereira, C. Cámara Hijón, I. Tovar García, S. Romero Chala, J.A. García Trujillo, I Mágriz Tascón
SECONDARY IMMUNODEFICIENCIES MAY PERFECTLY MIMIC PRIMARY IMMUNODEFICIENCIES
AZ. CALISKANER (1), S. SOYYIGIT (1), S. ARSLAN (1), R. UCAR (1)
SEEK, AND YE SHALL SEE: SIXTEEN CASES OF WISKOTT-ALDRICH SYNDROME DIAGNOSED IN JUST FOURS YEARS AT CHANDIGARH, NORTH INDIA
D Suri (1), A Rawat (1), B Saikia (2), R Minz (2), A Gupta (1), KW Chang (3), YL Lau (3), S Singh (1)
SEVERE COMBINED IMMUNE DEFICIENCY (SCID) NEWBORN SCREENING IN ONTARIO, CANADA: NOVEL SCREENING METHOD AND OUTCOMES OF THE FIRST 22 MONTHS
L. Gallagher (1), O.Y. Aldirbashi (1), D.E. Bulman (1,2), P. Chakraborty (1, 2)
SEVERE COMBINED IMMUNODEFICIENCY (SCID) IN VIETNAM: CLINICAL CHARACTERISTICS AND SURVIVAL OUTCOME.
H. Thuc (1), V.A. Nguyen, M.H. Le, Q.L. Nguyen
SEVERE HSV INFECTIONS WITH CONCOMITANT INFECTION WITH MYCOPLASMA PNEUMONIAE IN 17-YEAR-OLD PATIENT WITH PRIMARY IMMUNODEFICIENCY
A. Lewandowicz Uszynska (1), G. Pasternak (1), M. Zawierta (1)
SEVERE HYPOGAMMAGLOBULINEMIA IN ADULTS: CLINICAL AND ETIOLOGICAL PROFILE  IN AN INTERNAL MEDICINE UNIT.
G. CHALHOUB (1), F. AROUS, B. BENNET
SEVERE INFLAMMATORY BOWEL DISEASE AS THE MAIN MANIFESTATION  OF XIAP-DEFECT
A. Roppelt (1), T. Varlamova (4), E. Deripapa (1), E. Raykina (4), N. Shchigoleva (2), Yu. Dmitrieva (1), T. Gabrusskaya (3), A. Shcherbina (1)
SOUTH EAST ASIA PRIMARY IMMUNODEFICIENCIES (SEAPID) WPIW REGIONAL WALK-ABOUT CAMPAIGN: PHYSICIANS-STUDENTS-PATIENTS PARTNERSHIP INITIATIVE
A. Ali (1), S. Lai (2), B. Lim (3), K. Koh (3), F. Bakon (4), AH. AbdulLatiff (5), L. MNoh (1)
SPECTRUM OF PREDOMINANT ANTIBODY DEFECTS : TWENTY YEARS EXPERIENCE FROM SINGLE TERTIARY CARE CENTRE IN NORTH-WEST INDIA
S. Singh (1), A Rawat (1), D Suri (1), A Gupta (1), R Minz (2), B Saikia (2), K Chan (3), Y Lau (3), K Oshima (4), N Mitsuiki (4), O Ohara (4), C Kamae (5), K Honma (5), N Nakagawa (5), K Imai (5), S Nonoyama
STAT1 INBORN ERRORS IN MOROCCO: ABOUT 6 CASES
I. benhsaien (1), F. ailal (1), L. jeddane (1), J. najib (1), JL. casanova (2), A. puel (3), AA. bousfiha (1)
SWEDISH GUIDELINES FOR ASSESSMENT, DIAGNOSIS AND TREATMENT OF IMMUNODEFICIENCIES
N Brodszki (1), J Björkander (1), A Fasth (1), P Forsberg (1), V Friman (1), C Granert (1), L Hammarström (1), G Jönsson (1), L Marthinsen (1), H Matsols (1), A-C Norlin (1), S Oskarsdottir (1), K Pauksens (1), P Wågström (1), A Åhlin (1)
SWITCH FROM IVIG TO SCIG MAY RELIEVE THE BURDEN OF IMMUNOGLOBULIN REPLACEMENT THERAPY IN ADULT PATIENTS WITH PRIMARY IMMUNODEFICIENCY. LESSONS FROM THE VISAGES STUDY
Roland Jaussaud (1), Boris Bienvenu (2), Eric Hachulla (3), Cyrille Hoarau (4), Grégoire Cozon (5), Marlène Pasquet (6), Pierre Clerson (7), Jean-Charles Crave (8), Jean-Christophe Delain (8), Patrick Cherin (9)
THE DEVELOPMENT OF PERSISTENT HYPOGAMMAGLOBULINEMIA IN PATIENTS WITH ITP AFTER RITUXIMAB TREATMENT: UNMASKING OF COMMON VARIABLE IMMUNODEFICIENCY
S. Yoffe (1), N Marcus (1), N Segal (1), B Garty (1), J Yakobovich (1), H Tamary (1), Y Levy (1)
THE FIRST EXPERIENCE OF GENETIC DIAGNOSIS OF ATAXIA-TELANGIECTASIA IN UKRAINE.
I. Savchak (1), L. Kostyuchenko (1), H. Makukh (2)
THE LONG WAY UNTIL DIAGNOSIS
M. BATANEANT (1), C DOBRESCU (2), V TUDORACHE (1), E BOERIU (1), A ISAC (2), A PASCALAU (2), M BAICA (2), I COZMA (2), S ARGHIRESCU (1), M SERBAN (3)
THE PASSENGER STRAND, MIR-21-3P, IS UPREGULATED IN AN ALPS-FAS PATIENT
M. Teocchi (1), L. Furlaneto Marega (1), M. M. dos Santos Vilela (1)
THE PERFORMANCE OF A NEW HOMOGENEOUS PCR ASSAY FOR SCID SCREENING
P Ollikka (1), H-M Raussi (1), M Sjoroos (1), P Kerokoski (1), H Lindroos (1), P Huhtinen (1), K Mattila (1), A Ylikoski (1)
THE PURIFICATION OF IINTRAVENOUS IMMUNOGLOBULIN TO MANAGE THE POTENTIAL IMPACT ON PRODUCT TOLERANCE
S. Puget (1), P. Paolantonacci (2), C. de Coupade (2), P. Appourchaux (3), C. Michalski (3), L. Burlot (2)
THE REPORT OF TWO NOVEL GENE MUTATIONS IN WISKTT-ALDRICH SYNDROME
M. Badealzadeh (1), M.R. Fazlollahi (1), M. Houshmand (2), A.A. Hamidieh (3), B.S. Shamsian (4), R. Khademi (1), Z. Pourpak (1), M. Moin (1)
THE ROLE OF NUTRITION IN PEDIATRIC PRIMARY IMMUNO-DEFICIENCY DISEASE
J. Menang (1), Njimogu Samuel (2)
THE SOUL OF A NEW PUMP – SURPRISING EDUCATIONAL DISCOVERIES WHEN CREATING MEDICAL DEVICES WITH CLINICIANS AND USERS
B. Sealfon (1), C. Soderman (1)
THROMBOCYTOPENIA IN PEG-ADA-SCID PATIENT TREATED WITH MUD HCT TRANSPLANT: A CASE REPORT AND REVIEW OF LITERATURE
S. Sumayli (1), R Arnaout, F Sheikh, A Khaliq, H Hakami, G Aldosari, L Alshekaili, S Algazlan
THROMBOCYTOPENIA IN PEG-ADA-SCID PATIENT TREATED WITH MUD HCT TRANSPLANT: A CASE REPORT AND REVIEW OF LITERATURE
S. Sumayli (1), R Arnaout (2), F Sheikh (3), A Khaliq (4), G Aldosari (5), H Hakami (6), S Algazlan (7)
TNF SINGLE NUCLEOTIDE POLYMORPHISM IN PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY
V. Perovic (1), D. Perovic (2), R. Mijanovic (3), V. Pravica (1), B. Bonaci-Nikolic (3)
TREATMENT IN CVID COMPLICATED WITH INFLAMMATORY BOWEL DISEASE: HOW DIFFICULT IT CAN BE?
R. UCAR (1), S. ARSLAN (1), M. ASIL (2), S. SOYYIGIT (1), H. ATASEVEN (2), A.Z. CALISKANER (1)
TREATMENTS WITH INTRAVENOUS IMMUNOGLOBULINS AND ADVERSE EVENTS IN PRIMARY IMMUNODEFICIENCIES
S. Puget (1), L. Darnige (2)
TWO CLINICAL STUDIES EVALUATING THE PHARMACOKINETICS, SAFETY, AND EFFICACY OF A NEW HUMAN PLASMA-DERIVED INTRAVENOUS IMMUNOGLOBULIN (‘NEWGAM 10%’) IN PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASE
M. Borte, S. Wietek, B. Pyringer, T.E. Svae, J. Moy, I. Melamed
ULCERATIVE COLITIS AND AGRESSIVE COLORECTAL CANCER IN A YOUNG ADULT WITH X-LINKED AGAMMAGLOBULINEMIA
D. LIBERATORE (1), J. ETCHEVERS (2), J. DE PAULA (2), G. ROSSI (3), D ANDRESIK (4), A AGUIRRE (4), J SANTINO (5), M VERZURA (6)
UNBIASED TARGETED NEXT GENERATION SEQUENCING MOLECULAR APPROACH IN THE DIAGNOSIS OF PRIMARY IMMUNODEFICIENCY DISEASES
H. Al-Mousa (1), M. Abouelhoda, D. Monies, A. Al-Ghonaium,
N. Al-Tassan, B. Al-Saud, L. Al-Baik, H. Al-Dhekri, M. Dasouki, R. Arnaout,
N. Ades, S. Elshorbagi, S. Al-Muhsen, S. AlGazlan, M. El-Kalioby, S. Subhani, T. Faquih, S. Al-Hissi, B. Myere, A. Hawwari
VISAGES : A STUDY TO ASSESS THE QUALITY OF LIFE AND SATISFACTION OF CHILDREN WITH PRIMARY IMMUNODEFICIENCY DISEASE RECEIVING IMMUNOGLOBULIN REPLACEMENT THERAPY IN REAL-LIFE CONDITIONS
Marlène Pasquet (1), Roland Jaussaud (2), Boris Bienvenu (3), Eric Haculla (4), Patrick Cherin (5), Grégoire Cozon (6), Pierre Clerson (7), Jean-Charles Crave (8), Jean-Christophe Delain (8), Cyrille Hoarau (9)
WORKUP OF A PATIENT WITH CHRONIC MUCOCUTANEOUS CANDIDIASIS
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