Skip to content
B

B. Halimy

Publications (2)

Apert’s Disease: Three Case Reports and Review of the Literature

A. Ourrai, B. Halimy, A. Hassani, R. Abilkassem & A. Agadr · Asian Journal of Pediatric Research · 2024

Apert's disease is an acrocephalosyndactyly, which is part of the craniofaciostenosis group. It is characterized by craniofacial dysmorphia and syndactyly of the hands and feet. It is a rare autosomal dominant condition, but sporadic cases are common. The pathogenesis is poorly u...

Open access Research Article 10.9734/ajpr/2024/v14i2326