Autosomal dominant spastic ataxia 7 (SPAX7)
Evidence-based neurology checklist on autosomal dominant spastic ataxia 7 (spax7): Genetics The transmission is autosomal dominant Clinical features Synonym
Genetics
- The transmission is autosomal dominant
Clinical features
Synonym
References
- Dick DJ, Newman PK, Cleland PG. Hereditary spastic ataxia with congenital miosis: four cases in one family. Br J Ophthalmol 1983; 67:97-101.
- Timby N, Stattin EL, Kristiansen I, Eriksson U, Erikson A. Early onset autosomal dominant spinocerebellar ataxia with miosis: four cases. Eur J Paediatr Neurol 2008; 12:38-40.
Related checklists
- Autosomal dominant spastic ataxia (SPAX1)
- Autosomal recessive spastic ataxia 2 (SPAX2)
- Autosomal recessive spastic ataxia 3 (SPAX3)
- Autosomal recessive spastic ataxia 4 (SPAX4)
- Autosomal recessive spastic ataxia 5 (SPAX5)
- Autosomal recessive spastic ataxia 6 (SPAX6)
- Autosomal recessive spastic ataxia 8 (SPAX8)
- Galloway Mowat syndrome (GAMOS)
- PHARC syndrome
- Spastic ataxias: differential diagnosis
