Cataract, congenital nuclear autosomal recessive 1 is a rare condition of congenital cataract that is not associated with any other abnormality.This syndrome is recessive and the type 1 is caused by mutation on chromosome 19q13.
Some of the symptoms of cataract, congenital nuclear autosomal recessive 1:-
- Cataract
- Impaired vision
- Opacities in pupil
When should you consult a doctor?
Consult a doctor if you have signs of cataract, congenital nuclear autosomal recessive 1. Early diagnosis may help in quick recovery.
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