Poster
APSID Poster
APP1-1 Allo-immune Hemolytic Disease of the Newborn resulting from Rhesus Incompatibility -A Case Report
Presenter:
Lytheang Try
APP1-2 Efficacy of JAK inhibitors in Patients with STING-Associated Vasculopathy with Onset in Infancy
Presenter:
Mengyue Deng
APP1-3 Tocilizumab Effectively Managed for a Girl with A20 Haploinsufficiency.
Presenter:
Dae Chul Jeong
APP1-4 Identified mutation in FOXP3 gene in Vietnamese patient with IPEX syndrome
Presenter:
Mai Thi Phuong Nguyen
APP1-6 Short stature, hypothyroidism and systemic lupus erythematosus: clinical clues to an underlying type 1 interferonopathy
Presenter:
Prabal Barman
APP1-7 Elucidating the Impact of STAT1 Gain-of-Function Mutations: Immunophenotyping and Therapeutic Insights from Chronic Mucocutaneous Candidiasis Cases in Taiwanese Families
Presenter:
Wei Te Lei
APP2-1 Increasing trend of COVID-19 anti-S-RBD and surrogate neutralizing antibodies in X-linked agammaglobulinaemia patients receiving Ig replacement from 2021 to 2023
Presenter:
Jaime S Rosa Duque
APP2-2 Mild clinical phenotype of Omicron infection in children with inborn errors of immunity
Presenter:
Han Yang
APP2-3 Identification mutations of BTK Gene in patients with X-Linked Agammaglobulinemia Disease
Presenter:
Tien Manh Ngo
APP2-4 Predictors of infections in patients with secondary hypogammaglobulinemia in a tertiary rheumatological unit
Presenter:
Justina Wei Lynn Tan
APP2-5 Unmasking the Impact of STAT-1 Gain-of-Function Mutations
Presenter:
Brenda Guendulain velazquez
APP2-6 The first case of chronic osteomyelitis by fluconazole-resistant Candida albicans in a CARD-9 deficiency Korean patient
Presenter:
Yoonsun Yoon
APP3-1 A case of disseminated molluscum contagiosum in atopic triad with recurrent pneumonia and work-up of underlying combined immunodeficiency
Presenter:
Carolyn Mae Matira Abelador
APP3-2 Wiskott Aldrich Syndrome Suspected on a Critically-Ill 5 month-old Male
Presenter:
Jemma Grace Fianza
APP3-3 Successful allogeneic hematopoietic stem cell transplantation for a male with EBV associated-hemophagocytic lymphocystiocytosis and X-linked Inhibitor of Apoptosis Deficiency: a Case Report in Taiwan
Presenter:
CHING YU WANG
APP4-1 Clinical courses and genetic analysis in Taiwanese patients with Syndromic diarrhea/Trichohepatoenteropathy (SD/THE)
Presenter:
Wen-I Lee
APP4-3 Outcome for patients with severe congenital neutropenia treated outpatient granulocyte colony-stimulating factor at Vietnam National Children’s Hospital.
Presenter:
Anh Phuong Ha
APP4-5 Long road to recovery of one IFNGR1 deficiency case: from head to calf, from BCG to NTM
Presenter:
Yunfei An