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Congenital cataract: An ocular manifestation of classical homocystinuria

BACKGROUND: Homocystinuria is an autosomal recessive metabolic disorder occurring due to the defects in cystathionine‐β‐synthase enzyme. The study was carried out to investigate a Pakistani family presenting bilateral congenital cataract with symptoms of classical homocystinuria at LRBT Free Eye Hos...

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Detalles Bibliográficos
Autores principales:	Saba, Neelam, Irshad, Saba
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2021
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457696/ https://www.ncbi.nlm.nih.gov/pubmed/34342182 http://dx.doi.org/10.1002/mgg3.1742

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