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Bilaterally symmetrical isolated corectopia: a case report.

M Gangadharan, G Menon

Japanese Journal of Ophthalmology

|January 1, 1986

Summary

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This study reports a rare case of isolated congenital corectopia in a 15-year-old boy affecting both eyes. Autosomal recessive inheritance is suggested for this isolated eye condition.

Area of Science:

Ophthalmology
Medical Genetics

Background:

Congenital corectopia, a rare condition characterized by an upwardly displaced pupil, can occur in isolation or as part of various syndromes.
Understanding the genetic basis of isolated corectopia is crucial for genetic counseling and further research into ocular development.

Observation:

A 15-year-old male presented with symmetrical corectopia in both eyes as an isolated finding.
No other ocular or systemic abnormalities were noted in the patient.

Findings:

The case suggests an isolated congenital corectopia, presenting bilaterally and symmetrically.
The pattern of occurrence in the family, though not detailed, points towards a potential autosomal recessive mode of inheritance.

Implications:

Related Experiment Videos

This case contributes to the understanding of isolated congenital corectopia and its potential genetic underpinnings.
Further investigation into the genetic factors responsible for isolated corectopia may reveal novel pathways in ocular development and disease.