Vici Syndrome: A Case Report of Non-Identical Twins with Oculo- Cutaneous Albinism, Recurrent Infections and Absent Corpus Collasum
- International Journal of Vaccines & Vaccination
-
Rayan Goda1*, Ahlam Abdalrahman2, Nahla H Erwa3 and Sahar3
Soba University Hospital, Sudan - Ahlam Abdalrahman, Department of Paediatrics, Soba University Hospital, Sudan
- Nahla H Erwa, Immunology Department, Soba University Hospital, Sudan
- Sahar, Immunology Department, Soba University Hospital, Sudan
Abstract
Vici syndrome is a rapidly progressive, neurological disease of childhood. It is associated with complete agenesis of the corpus collasum, occulocutaneous albinism, immunodeficiency, cardiomyopathy and neuromuscular defects. This a case report of non identical twins who presented with failure to thrive, seizures, developmental delay associated with albinism, absent corpus collasum, and recurrent infections.
Keywords
Vici Syndrome, Albinism, Immunodeficiency, Absent corpus collasum, Seizures, Developmental delay, Infections, Complete Blood Count, Severe Combined Immunodeficiency, Electroencephalogram, Magnetic Resonance Imaging, Peripheral Blood Picture, Immunoglobulin Gamma-2, Non identical twins, Cardiomyopathy
