About The Contact Registry
The Contact Registry is a method by which patients (and their families) can register themselves to be contacted in the future about clinical research opportunities. An online Registry form exists for all the CRC-SCA disorders currently being studied:
-
Spinocerebellar ataxia:
- Ataxia telangiectasia
- Ataxia with oculomotor apraxia (AOA) type 1
- Ataxia with oculomotor apraxia (AOA) type 2
- Ataxia with vitamin E deficiency (AVED)
- Ataxia, unknown cause
- Autosomal recessive ataxia of Charlevoix-Saguenay (ARSACS)
- Dentatorubral-pallidoluysian atrophy (DRPLA)
- Fragile X tremor-ataxia syndrome (FXTAS)
- Friedreich's ataxia
- GAD ataxia
- Gluten ataxia
- Mitochondrial ataxia
- Mitochondrial recessive ataxia syndrome (MIRAS; POLG mutation)
- Multiple system atrophy-cerebellar type (MSA-C)
- Olivopontocerebellar atrophy (OPCA)
- Paraneoplastic ataxia
- Spinocerebellar ataxia 1(SCA1)
- Spinocerebellar ataxia 2(SCA2)
- Spinocerebellar ataxia 3(SCA3/Machado Joseph disease/MJD)
- Spinocerebellar ataxia 4(SCA4)
- Spinocerebellar ataxia 5(SCA5)
- Spinocerebellar ataxia 6(SCA6)
- Spinocerebellar ataxia 7(SCA7)
- Spinocerebellar ataxia 8(SCA8)
- Spinocerebellar ataxia 10(SCA10)
- Spinocerebellar ataxia 11(SCA11)
- Spinocerebellar ataxia 12(SCA12)
- Spinocerebellar ataxia 13(SCA13)
- Spinocerebellar ataxia 14(SCA14)
- Spinocerebellar ataxia 15(SCA15)
- Spinocerebellar ataxia 16(SCA16)
- Spinocerebellar ataxia 17(SCA17)
- Spinocerebellar ataxia 18(SCA18)
- Spinocerebellar ataxia 19(SCA19)
- Spinocerebellar ataxia 20(SCA20)
- Spinocerebellar ataxia 21(SCA21)
- Spinocerebellar ataxia 22(SCA22)
- Spinocerebellar ataxia 23(SCA23)
- Spinocerebellar ataxia 24(SCA24); SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4
- Spinocerebellar ataxia 25(SCA25)
- Spinocerebellar ataxia 26(SCA26)
- Spinocerebellar ataxia 27(SCA27)
- Spinocerebellar ataxia 28(SCA28)
- Spinocerebellar ataxia 29(SCA29)
- Spinocerebellar ataxia 31(SCA31)
- Sporadic ataxia (onset before 20 years)
- Sporadic ataxia (onset between 20-50 years)
- Sporadic ataxia (onset after 50 years)
Department of Health and Human Services
National Institutes of Health
The Clinical Research Consortium for Spinocerebellar Ataxias (CRC-SCA) is a member of the Rare Diseases Clinical Research Network, which is funded by the National Institutes of Health.