Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja Crandall syndrome is characterized by progressive sensorineural deafness, alopecia and hypogonadism with LH and GH deficiencies. It has been described in three brothers. It resembles Björnstad's syndrome (see this term) that combines irregular pili torti and deafness. It is probably inherited as and autosomal recessive disorder. Disease data Klasyfikacja Disease Synonimy Alopecia-deafness-hypogonadism syndrome Zespół łysienia, głuchoty i hipogonadyzmu Alopecia-hearing loss-hypogonadism syndrome Alopecia-sensorineural deafness-hypogonadism syndrome Alopecia-sensorineural hearing loss-hypogonadism syndrome Kod ORPHA 202 Kod OMIM - Kod ICD10 - Kod ICD11 - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl