Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome

Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome is characterized by congenital muscular dystrophy, infantile cataract and hypogonadism. It has been described in seven individuals from an isolated Norwegian village and in one unrelated individual. Transmission appears to be autosomal recessive.

Also known as: Bassoe syndrome, benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract, familial congenital muscular dystrophy with gonadal dysgenesis, muscular dystrophy, congenital, infantile with cataract and hypogonadism, muscular dystrophy, congenital, with infantile cataract and hypogonadism

5 clinical trials for this condition and its sub-types, 0 tagged with Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome itself.