A. Baaziz

Langerhans Cell Histiocytosis Associated with EVANS Syndrome: A Case Report

A. Baaziz, A. Ourrai, A. Hassani, A. Radi & R. Abilkassem · Asian Journal of Pediatric Research · 2025

Introduction :  Langerhans cell histiocytosis (LCH) is a rare clonal disorder of dendritic cells with heterogeneous clinical manifestations, ranging from isolated bone lesions to severe multisystemic disease. Its association with Evans syndrome, defined by autoimmune haemolytic a...

Open access Research Article 10.9734/ajpr/2025/v15i9474

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