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Article

Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.

American journal of human genetics - 1 Oct 1995

Padma T, Ayyagari R, Murty J S, Basti S, Fletcher T, Rao G N, Kaiser-Kupfer M, Hejtmancik J F

Abstract excerpt

Congenital cataracts constitute a morphologically and genetically heterogeneous group of diseases that are a major cause of childhood blindness. Different loci for hereditary congenital cataracts have been mapped to chromosomes 1, 2, 16, and 17q24. We report linkage of a gene causing a unique form of autosomal dominant zonular cataracts with Y-sutural opacities to chromosome 17q11-12 in a three-generation family...

Topics

Adolescent
Cataract
Chromosomes, Human, Pair 17
Genetic Linkage
Genotype
Humans
Lod Score
Male
Pedigree

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7573044
PMCID: PMC1801479

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7573044-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.PMID 7573044Read ↗

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