Gemignani syndrome

Orpha code: 2074OMIM code:

Definition

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
Classification

Malformation syndrome

Synonyms
Spinocerebellar ataxia-amyotrophy-deafness syndrome
Ataksja móżdżkowo-rdzeniowa - amiotrofia - głuchota
Spinocerebellar ataxia-amyotrophy-hearing loss syndrome
ORPHA code
2074
OMIM code
-
ICD10 code
-
ICD11 code
-

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl