Cataract-deafness-hypogonadism syndrome

Cataract-deafness-hypogonadism syndrome is an extremely rare multiple congenital abnormality syndrome, described in only three brothers to date, that is characterized by the association of congenital cataract, sensorineural deafness, hypogonadism, mild intellectual deficit, hypertrichosis, and short stature. There have been no further descriptions in the literature since 1995.

Also known as: Schaap-Taylor-Baraitser syndrome, cataracts, sensorineural deafness, hypogonadism, hypertrichosis and short stature

0 clinical trials for this condition and its sub-types, 0 tagged with Cataract-deafness-hypogonadism syndrome itself.