A Rare Case of Childhood Glaucoma Resulting from Anterior Segment Dysgenesis Associated with a Homozygous Mutation in the CPAMD8 Gene

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Publication Details

Journal
Genes
Published
2026-04-21
DOI
https://doi.org/10.3390/genes17040494
Primary Topic
Glaucoma and retinal disorders
Type
article
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article

A Rare Case of Childhood Glaucoma Resulting from Anterior Segment Dysgenesis Associated with a Homozygous Mutation in the CPAMD8 Gene

R Kaneva, Kunka Kamenarova, Kalina Mihova, Stanislava Kostova et al.
Genes
Glaucoma and retinal disorders
article

A Rare Case of Childhood Glaucoma Resulting from Anterior Segment Dysgenesis Associated with a Homozygous Mutation in the CPAMD8 Gene

R Kaneva, Kunka Kamenarova, Kalina Mihova, Stanislava Kostova, Alexander Oscar, Kiril Genov, Nevyana Veleva-Krasteva, Yoanna Kaneva
article en

Abstract

No abstract available for this paper.
GenesVol. 17(4)
Alexandrovska Hospital (BG), Medical University of Sofia (BG)
Good health and well-being
Openalex Percentile: Top 13%
Glaucoma and retinal disorders
DOIOpen Access PDFOpenAlex
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