ATAXIA neurology checklists
Explore evidence-based neurology topics and fully referenced clinical checklists covering ATAXIA.
Ataxia: genetic classifications
Freidreich's ataxia (FA)
Ataxia with oculomotor apraxia (AOA)
Miscellaneous autosomal recessive ataxias
- Ataxia telangiectasia (AT)
- Ataxia-telangiectasia like disorder (ATLD)
- COQ8A ataxia
- Cayman ataxia
- Cockayne syndrome
- Autosomal recessive spinocerebellar ataxia with raised alpha-fetoprotein
- Abetalipoproteinaemia
- Gordon Holmes syndrome (GHS)
- Autosomal recessive spinocerebellar ataxias (SCAR)
- Autosomal recessive cerebellar ataxia with STUB1 mutations
- Spinocerebellar ataxia with axonal neuropathy (SCAN1)
- Infantile-onset spinocerebellar ataxia (IOSCA)
Spinocerebellar ataxias (SCA): 1-24
- Spinocerebellar ataxia (SCA) summary of key features
- Spinocerebellar ataxia type 1 (SCA 1)
- Spinocerebellar ataxia type 2 (SCA2)
- Spinocerebellar ataxia type 3 (SCA3): clinical features
- Spinocerebellar ataxia type 3 (SCA3): management
- Spinocerebellar ataxia type 4 (SCA4)
- Spinocerebellar ataxia type 5 (SCA5)
- Spinocerebellar ataxia type 6 (SCA6)
- Spinocerebellar ataxia type 7 (SCA7)
- Spinocerebellar ataxia type 8 (SCA8)
- Spinocerebellar ataxia type 9 (SCA9)
- Spinocerebellar ataxia type 10 (SCA10)
- Spinocerebellar ataxia type 11 (SCA11)
- Spinocerebellar ataxia type 12 (SCA12)
- Spinocerebellar ataxia type 13 (SCA13)
- Spinocerebellar ataxia type 14 (SCA14)
- Spinocerebellar ataxia type 15 (SCA15)
- Spinocerebellar ataxia type 16 (SCA16)
- Spinocerebellar ataxia type 17 (SCA17)
- Spinocerebellar ataxia type 18 (SCA18)
- Spinocerebellar ataxia type 19 (SCA19)
- Spinocerebellar ataxia type 20 (SCA20)
- Spinocerebellar ataxia type 21 (SCA21)
- Spinocerebellar ataxia type 22 (SCA22)
- Spinocerebellar ataxia type 23 (SCA23)
- Spinocerebellar ataxia type 24 (SCA24)
Spinocerebellar ataxias (SCA): 25-50
- Spinocerebellar ataxia type 25 (SCA25)
- Spinocerebellar ataxia type 26 (SCA26)
- Spinocerebellar ataxia type 27A (SCA27A)
- Spinocerebellar ataxia type 28 (SCA28)
- Spinocerebellar ataxia type 29 (SCA29)
- Spinocerebellar ataxia type 30 (SCA30)
- Spinocerebellar ataxia type 31 (SCA31)
- Spinocerebellar ataxia type 32 (SCA32)
- Spinocerebellar ataxia type 33 (SCA33)
- Spinocerebellar ataxia type 34 (SCA34)
- Spinocerebellar ataxia type 35 (SCA35)
- Spinocerebellar ataxia type 36 (SCA36)
- Spinocerebellar ataxia type 37 (SCA37)
- Spinocerebellar ataxia type 38 (SCA38)
- Spinocerebellar ataxia type 39 (SCA39)
- Spinocerebellar ataxia type 40 (SCA40)
- Spinocerebellar ataxia type 41 (SCA41)
- Spinocerebellar ataxia type 42 (SCA42)
- Spinocerebellar ataxia type 43 (SCA43)
- Spinocerebellar ataxia type 44 (SCA44)
- Spinocerebellar ataxia type 45 (SCA45)
- Spinocerebellar ataxia type 46 (SCA46)
- Spinocerebellar ataxia type 47 (SCA47)
- Spinocerebellar ataxia type 48 (SCA48)
- Spinocerebellar ataxia type 49 (SCA49)
- Spinocerebellar ataxia type 50 (SCA50)
- Spinocerebellar ataxia type 27B (SCA27B)
Episodic ataxias (EA)
- Episodic ataxia (EA) summary of key features
- Episodic ataxia type 1 (EA1)
- Episodic ataxia type 2 (EA2)
- Episodic ataxia type 3 (EA3)
- Episodic ataxia type 4 (EA4)
- Episodic ataxia type 5 (EA5)
- Episodic ataxia type 6 (EA6)
- Episodic ataxia type 7 (EA7)
- Episodic ataxia type 8 (EA8)
- Episodic ataxia (EA): differential diagnosis
Miscellaneous autosomal dominant ataxias
Fragile X tremor ataxia syndrome (FXTAS)
Miscellaneous X linked ataxias
Spastic ataxias
- 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 dominant spastic ataxia 7 (SPAX7)
- Autosomal recessive spastic ataxia 8 (SPAX8)
- Galloway Mowat syndrome (GAMOS)
- PHARC syndrome
- Spastic ataxias: differential diagnosis
