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Article

Genetics of Bietti Crystalline Dystrophy.

Asia-Pacific journal of ophthalmology (Philadelphia, Pa.) - 1 Jan 2000

Ng Danny S C, Lai Timothy Y Y, Ng Tsz Kin, Pang Chi Pui

Abstract excerpt

Bietti crystalline dystrophy (BCD) is an inherited retinal degenerative disease characterized by crystalline deposits in the retina, followed by progressive atrophy of the retinal pigment epithelium (RPE), choriocapillaris, and photoreceptors. CYP4V2 has been identified as the causative gene for BCD. The CYP4V2 gene belongs to the cytochrome P450 superfamily and encodes for fatty acid ω-hydroxylase of both...

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Share to Corneal Dystrophies, Hereditary
Share to Cytochrome P450 Family 4
Share to Electroretinography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Endoplasmic Reticulum

Share to Retinal Cone Photoreceptor Cells

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Share to Retinal Pigment Epithelium

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Source

Identifiers

PMID: 27228076
DOI: 10.1097/APO.0000000000000209

Genes

RPE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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