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Geographical Variability in CYP1B1 Mutations in Primary Congenital Glaucoma

Primary congenital glaucoma (PCG) is a rare type of glaucoma that is inherited in an autosomal recessive manner. PCG can lead to blindness if not detected early in children aged 3 or younger. PCG varies in presentation among various populations, where disease presentation and disease severity vary b...

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Detalles Bibliográficos
Autores principales: Shah, Manali, Bouhenni, Rachida, Benmerzouga, Imaan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8999900/
https://www.ncbi.nlm.nih.gov/pubmed/35407656
http://dx.doi.org/10.3390/jcm11072048

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