 |
|
Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
| Enter a medical term |
| Spinocerebellar Ataxias | Legal notice |
Other terms
Ataxia, Spinocerebellar,Ataxias, Spinocerebellar,Spinocerebellar Ataxia,Dominantly-Inherited Spinocerebellar Ataxias,Ataxia, Dominantly-Inherited Spinocerebellar,Ataxias, Dominantly-Inherited Spinocerebellar,Dominantly Inherited Spinocerebellar Ataxias,Dominantly-Inherited Spinocerebellar Ataxia,Spinocerebellar Ataxia, Dominantly-Inherited,Spinocerebellar Ataxias, Dominantly-Inherited,Spinocerebellar Ataxias, Dominantly Inherited,Spinocerebellar Atrophies,Atrophies, Spinocerebellar,Atrophy, Spinocerebellar,Spinocerebellar Atrophy,Spinocerebellar Ataxia Type 1,Type 1 Spinocerebellar Ataxia,Spinocerebellar Ataxia-1,Spinocerebellar Ataxia 1,Spinocerebellar Ataxia Type 6,Type 6 Spinocerebellar Ataxia,Spinocerebellar Ataxia-6,Spinocerebellar Ataxia 6,Spinocerebellar Ataxia Type 4,Type 4 Spinocerebellar Ataxia,Spinocerebellar Ataxia-4,Spinocerebellar Ataxia 4,Spinocerebellar Ataxia Type 5,Type 5 Spinocerebellar Ataxia,Spinocerebellar Ataxia-5,Spinocerebellar Ataxia 5,Spinocerebellar Ataxia Type 7,Type 7 Spinocerebellar Ataxia,Spinocerebellar Ataxia-7,Spinocerebellar Ataxia 7,Spinocerebellar Ataxia Type 2,Type 2 Spinocerebellar Ataxia,Spinocerebellar Ataxia-2,Spinocerebellar Ataxia 2
Description
Spinocerebellar Ataxias: A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
Pervious tree
Next tree
Other locations in tree
- Cerebellar Ataxia
- Spinocerebellar Degenerations
- Spinocerebellar Degenerations
- Spinocerebellar Degenerations
- Spinocerebellar Degenerations
Legal notice
The U.S. National Library of Medicine is the creator, maintainer, and provider of the data above.
The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
Neither the United States Government, nor any of its agencies, contractors, subcontractors or employees makes any warranties, expressed or implied, with respect to data contained in the database, and, furthermore, assumes no legal liability for any party's use, or the results of such use, of any part of the database.
You will not assert any proprietary rights to any portion of the database, or represent the database or any part thereof to anyone as other than a United States Government database.
The MeSH data carry an international copyright outside the United States, its Territories or Possessions. These terms and conditions are in effect as long as the user retains any of the MeSH data obtained from this site.