Geroderma Osteodysplasticum Associated with Severe Factor V Deficiency in a Pediatric Patient: A Case Report
R. Acharafi, S. Sabbar, A. Baaziz & A. MDAGHRI ALAOUI · Asian Journal of Pediatric Research · 2026
Background: Geroderma osteodysplasticum (GO) is a rare autosomal recessive connective tissue disorder caused by variants in GORAB (golgin, RAB6 interacting), located on chromosome 1q24.2. The phenotype may mimic Ehlers–Danlos syndrome (EDS) or hereditary cutis laxa. Case Presenta...
Open access
Research Article
10.9734/ajpr/2026/v16i3529