The familial contribution to non-syndromic ocular coloboma in south India.
AIMS: To identify the proportion of familial cases of isolated ocular colobomatous malformations in a case series from south India. METHODS: Children with ocular coloboma without systemic features were recruited from multiple sources in Andhra Pradesh, India. Their families were traced, pedigrees drawn, and family members examined. RESULTS: 56 probands, 25 females (44.6%) and 31 males (57.4%) with a colobomatous malformation were identified. In 12 cases (21.4%) another family member was affected. The risk to siblings was 3.8%. The parents were consanguineous in 25 cases (44.6%). CONCLUSIONS: 21.4% of cases of isolated ocular coloboma in this highly consanguineous population of south India were familial, with both autosomal dominant and autosomal recessive mechanisms likely in different families.
Item Type | Article |
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Keywords | Adolescent, Child, Child, Preschool, Coloboma/complications/epidemiology/*genetics, Consanguinity, *Family Health, Female, Human, India/epidemiology, Male, Pedigree, Risk Factors, Siblings, Support, Non-U.S. Gov't, Adolescent, Child, Child, Preschool, Coloboma, complications, epidemiology, genetics, Consanguinity, Family Health, Female, Human, India, epidemiology, Male, Pedigree, Risk Factors, Siblings, Support, Non-U.S. Gov't |
ISI | 181368500022 |
Explore Further
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1771576 (OA Location)
- 10.1136/bjo.87.3.336 (DOI)
- 12598450 (PubMed)