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Safae Abdessadek

Publications (1)

Early-Onset Seizures Revealing 1p36 Deletion Syndrome in an Infant with Craniofacial Dysmorphism and Optic Disc Coloboma: A Case Report

Safae Abdessadek, Azzeddine Laaraje, Abdelilah Radi & Rachid Abilkassem · Asian Journal of Pediatric Research · 2026

Aims: To describe an infant in whom early-onset seizures led to the diagnosis of 1p36 deletion syndrome and to emphasise the diagnostic contribution of whole-exome sequencing with copy-number variation analysis when the early phenotype is incomplete. Presentation of Case: A 2-mon...

Open access Research Article 10.9734/ajpr/2026/v16i10577