Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja Gemignani syndrome is a rare neurodegenerative disease characterized by slowly progressive ataxia, amyotrophy of the hands and distal arms, spastic paraplegia, progressive sensorineural hearing loss, hypogonadism and short stature. Additional features include generalized cerebellar atrophy and peripheral nervous system anomalies. Small cervical spinal cord, intellectual/language disability and localized vitiligo have also been reported. There have been no further descriptions in the literature since 1989. Disease data Klasyfikacja Malformation syndrome Synonimy Spinocerebellar ataxia-amyotrophy-deafness syndrome Ataksja móżdżkowo-rdzeniowa - amiotrofia - głuchota Spinocerebellar ataxia-amyotrophy-hearing loss syndrome Kod ORPHA 2074 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