Gemignani syndrome

Orpha code: 2074OMIM code:

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
-

No additional description.

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