Crandall syndrome

This syndrome is characterized by progressive sensorineural deafness, alopecia and hypogonadism with LH and GH deficiencies. It has been described in three brothers. It resembles Bjrnstad's syndrome that combines irregular pili torti and deafness. It is probably inherited as and autosomal recessive disorder.

Also known as: alopecia-deafness-hypogonadism syndrome, alopecia-sensorineural deafness-hypogonadism syndrome, alopecia deafness hypogonadism

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