A. Laaraj

A Novel Homozygous HERC2 c.4660C>T (p. Arg1554Ter) Variant in an Infant with Severe Neurodevelopmental Disorder and Diffuse Osteopenia: A Case Report

Abdillahi Moustapha, A. Laaraj, A. Radi & R. Abikassem · Asian Journal of Pediatric Research · 2026

Background: HERC2-related intellectual developmental disorder is a rare autosomal recessive neurodevelopmental condition, and its full phenotypic spectrum remains incompletely defined. Case Presentation: We report a 7-month-old female infant born to second-degree consanguineous p...

Open access Research Article 10.9734/ajpr/2026/v16i10582

Prevalence and Clinical Features of Glaucoma in Pediatric Mucopolysaccharidosis Type I: A Retrospective Descriptive Study

Y. Achegri, A. Bouimtarhan, S. Azib, C. Bouabbadi, I. Jeddou, A. El Khoyaali, A. Fiqhi, Y. Mouzari, S. Ait Hmadouch, A. Radi, A. Laaraj & R. Abilkassem · Asian Journal of Advanced Research and Reports · 2025

Objective: To evaluate the prevalence, clinical characteristics, diagnostic challenges, and therapeutic outcomes of glaucoma in children diagnosed with mucopolysaccharidosis type I          (MPS I). Methods: A retrospective descriptive study was conducted on 12 pediatric patients...

Open access Research Article 10.9734/ajarr/2025/v19i111212