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Author

A. Marques-de-Faria

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Case report Open access Sep 2026

First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant.

Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%-5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce i...

Gabriela Roldão Correia-Costa, J. R. M. Prota, A. Marques-de-Faria et al. · 0 citations

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