Category: Immunodeficiency: primary or acquired

F.67 - Icf Syndrome Due to a Homozygous Mutation in dnmt3b Gene in Two Patients with Profound Hypogammaglobulinemia Without Facial Dysmorphism

Friday, Jun 16
6:15 PM – 7:30 PM

Roger Colobran Oriol

Immunology Division, Hospital Universitari Vall d'Hebron / Department of Cell Biology, Physiology and Immunology, Universitat Autonoma de Barcelona
Barcelona, Catalonia, Spain

Rosario Diez

Clinician (Pediatrics)
Pediatrics Unit, Hospital de Mataró, Consorci Sanitari de Mataró, Catalunya (Spain).
Mataro, Catalonia, Spain

Clara Franco-Jarava

Immunology Division, Hospital Universitari Vall d'Hebron
Barcelona, Catalonia, Spain

Marina Garcia-Prat

Research Assistant
Hospital Universitari Vall d'Hebron
Barcelona, Catalonia, Spain

Lourdes Garcia-Rodriguez

Clinician (Pediatrics)
Pediatric Unit, Hospital de Mataró, Consorci Sanitari de Mataró, Catalunya (Spain).
Mataró, Catalonia, Spain

Manuel Hernandez-González

Head of Immunology Division
Immunology Division, Hospital Universitari Vall d'Hebron / Department of Cell Biology, Physiology and Immunology, Universitat Autonoma de Barcelona
Barcelona, Catalonia, Spain

Andrea Martin-Nalda

Clinician on Clinical Immunology and Infectious Diseases (Pediatric)
Clinical Immunologist and Infectious Diseases (Pediatric), Hospital Universitari Vall d'Hebron
Barcelona, Catalonia, Spain

Pere Soler-Palacin

Consultant on Clinical Pediatric Immunology and Infectious Diseases
Pediatrics Division, Hospital Universitari Vall d'Hebron / Jeffrey Modell Diagnostic and Research Center for Primary Immunodeficiencies, Barcelona, Catalunya
Barcelona, Catalonia, Spain

Ricardo Pujol Borrell

Professor
Immunology Division, Hospital Universitari Vall d'Hebron / Department of Cell Biology, Physiology and Immunology, Universitat Autonoma de Barcelona
Barcelona, Catalonia, Spain