Cargando…
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...
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 |
Ejemplares similares
-
CYP1B1 mutations in Spanish patients with primary congenital glaucoma: phenotypic and functional variability
por: Campos-Mollo, Ezequiel, et al.
Publicado: (2009) -
Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma
por: García-Antón, María T., et al.
Publicado: (2017) -
CYP1B1-mediated Pathobiology of Primary Congenital Glaucoma
por: Faiq, Muneeb A, et al.
Publicado: (2015) -
Investigation of CYP1B1 mutations in Chinese patients with primary congenital glaucoma
por: Yang, Mei, et al.
Publicado: (2009) -
Targeted Screening for Predominant CYP1B1 Mutations in Primary Congenital Glaucoma
por: Sarfarazi, Mansoor
Publicado: (2018)