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Article

Clinical and Genetic Insights into Angelman Syndrome: A Retrospective Study of 26 Cases in Morocco.

Journal of molecular neuroscience : MN - 20 Jul 2026

Ouskri Amal, Abdelhamid Bouramtane, Hanae Daha Belghiti, Mohammed Ahakoud, Laila Bouguenouch, Karim Ouldim

Abstract excerpt

Angelman syndrome (OMIM #105830) is a rare neurodevelopmental disorder caused by loss of function of the maternally inherited UBE3A gene within the imprinted 15q11.2-q13 region. Although its clinical and molecular characteristics have been well described in European and Asian populations, data from low- and middle-income countries remain scarce. This retrospective study aimed to characterize the clinical and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 42474857
DOI: 10.1007/s12031-026-02570-5

Genes

UBE3A

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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