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 |
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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 |