Aicardi syndrom

Nordin, Massita and Mohd Mutalip, Siti Syairah and Jusoh, Siti Azma and Hussin, Siti Nooraishah and Jahidin, Aisyah Hasyila (2025) Aicardi syndrom. Prescription (5).

Abstract

Aicardi syndrom is caused by abnormalities in genes linked to brain development. It is an X-linked dominant condition, predominantly affecting females. Males with the mutation are unlikely to survive. This rare congenital neurological condition occurs in one in 100,000 live births in the United States, one in 93,000 in the Netherlands, and one in 110,000 in Northern Ireland. Approximately 1,000 cases have been documented in the United States, with an estimated 4,000 cases reported globally. Currently, there is no comprehensive data or published research on the incidence or prevalence of Aicardi syndrome in Malaysia.

Metadata

Item Type: Article
Creators:
Creators
Email / ID Num.
Nordin, Massita
UNSPECIFIED
Mohd Mutalip, Siti Syairah
UNSPECIFIED
Jusoh, Siti Azma
UNSPECIFIED
Hussin, Siti Nooraishah
UNSPECIFIED
Jahidin, Aisyah Hasyila
UNSPECIFIED
Subjects: Q Science > QH Natural history - Biology > Genetics > Human genetics
Q Science > QH Natural history - Biology > Genetics > Human genetics > Malaysia
Q Science > QH Natural history - Biology > Genetics > Genomics
Divisions: Universiti Teknologi MARA, Selangor > Puncak Alam Campus > Faculty of Pharmacy
Journal or Publication Title: Prescription
Number: 5
Keywords: Aicardi syndrome, brain abnormalities, respiratory, heart conditions
Date: May 2025
URI: https://ir.uitm.edu.my/id/eprint/118413
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