CATCN2 (medical condition): A rare recessively inherited type of congenital cataract that is not associated with any other abnormality. Type 2 is caused by a mutation in the beta-B3 crystallin gene on chromosome 22q11.2-q12.2.
See also:
Cataract, congenital nuclear, autosomal recessive 2:
»Introduction: Cataract, congenital nuclear, autosomal recessive 2
»Symptoms of Cataract, congenital nuclear, autosomal recessive 2
CATCN2: Another name for Cataract, congenital nuclear, autosomal recessive 2 (or close medical condition association).
»Introduction: Cataract, congenital nuclear, autosomal recessive 2
»Symptoms of Cataract, congenital nuclear, autosomal recessive 2
Some of the symptoms of CATCN2 incude:
Read more about symptoms of CATCN2 (Cataract, congenital nuclear, autosomal recessive 2)
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