Poster
IEI Poster
IEIP-A-1 A novel IKBKG intronic splicing mutation resulting in a completely loss of NEMO protein and causing a severe NEMO-ID phenotype
Presenter:
zhirui Tian
IEIP-A-2 A rare case of necrotizing encephalopathy in a CMV-infected boy with pancytopenia and abnormalities of skin, nails, and oral mucosa.
Presenter:
Tin Ngoc Nguyen
IEIP-A-3 Severe combined immunodeficiency in CHARGE syndrome, the first case in Korea
Presenter:
Luli Kim
IEIP-A-5 Tricho-Hepato-Enteric syndrome type 2: the first case report in Taiwan
Presenter:
Jou-An Chen
IEIP-B-5 Nephrocalcinosis in Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED); Primary or Iatrogenic?
Presenter:
Mohammadreza Shafiei
IEIP-C-1 Successful treatment of sirolimus for chronic diarrhea in LRBA Deficiency patient : A case report
Presenter:
Natcharindhorn Thaweepolaungsuchawon
IEIP-C-3 Immunodysregulation and lymphoproliferation in a patient with PIK3CD despite sirolimus use
Presenter:
Qin Ying Lim
IEIP-C-4 Early onset autoimmunity in patients with Inborne errors of Immunity
Presenter:
MADHUBALA SHARMA
IEIP-D-3 Recurrent flare-associated urticaria in adenosine deaminase type 2 deficiency
Presenter:
Pratap Kumar Kumar Patra
IEIP-D-5 Clinical and molecular profile of 20 patients with DOCK8 deficiency: A single-centre experience from Southern India
Presenter:
Neha Singh
IEIP-D-6 Newborn Screening for Primary Immunodeficiency Diseases (PID) in Malaysia: Current Status, Challenges and Progress
Presenter:
Wai Leng Chang
IEIP-E-2 A Teenage Girl with Severe Tuberculosis Complicated with Aspergillosis and Candidiasis
Presenter:
Fahreza Aditya Neldy
IEIP-E-3 Vast yet naïve. BENTA disease, an unusual presentation of extensive lymphoproliferation with CARD11 gain-of-function mutation.
Presenter:
Kent Mun Loh
IEIP-E-4 A unique clinical phenotype of IKBKG (nuclear factor-κB essential modulator) mutation presenting as severe central nervous system Aspergillus terreus infection
Presenter:
Lin Lin Liu
IEIP-E-5 CARD9 deficiency with allergic bronchopulmonary aspergillosis (ABPA)-like presentation: a case report
Presenter:
Mohammadreza Shafiei
IEIP-F-1 INFANT WITH CHRONIC GRANULOMATOUS DISEASE ASSOCIATED INTESTINAL PERFORATION: A NEW ASSOCIATION?
Presenter:
RAJKUMAR KUNDAVARAM
IEIP-F-2 A zebra or a unicorn- a Chinese boy with McLeod Phenotype Chronic Granulomatous Disease (CGD)
Presenter:
Ki Crystal LAm
IEIP-F-3 An interesting case of CYBB mutation in a Malay boy with normal maternal DHR oxidation test and matched mother-child HLA haplotype
Presenter:
Wan Fadhilah Wan Ibrahim
IEIP-F-4 Targeted next-generation sequencing reveals a novel variant in FERMT3 gene in a young girl with recurrent infections and epistaxis
Presenter:
Amit Kumar
IEIP-F-5 Genomic approach to diagnose Primary Immunodeficiency Diseases (PIDs) in Bangladeshi Children
Presenter:
Sudipta Roy
IEIP-F-6 Paediatric Immunologists’ Perspectives on Haematopoietic Stem Cell Transplantation (HSCT) for Primary Immunodeficiency Diseases (PID) in Malaysia
Presenter:
Mohammad Shukri Khoo