- ataxia central
- f.central ataxia.
Spanish-English dictionary. 2013.
ataxia central
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Central pontine myelinolysis — Classification and external resources Pons labeled at bottom left ICD 10 G … Wikipedia
ataxia hereditaria — Grupo de enfermedades hereditarias degenerativas de la médula espinal, cerebelo y, a menudo, de otras partes del sistema nervioso central, caracterizadas por temblor, espasmo, atrofia muscular, cambios esqueléticos y alteraciones sensitivas, que… … Diccionario médico
ataxia de Marie — una enfermedad hereditaria del sistema nervioso central con ataxia cerebelosa causada por una atrofia cortical bilateral del cerebelo. La enfermedad se inicia en la edad adulta. Los síntomas son una marcha espástica atáxica, mala coordinación de… … Diccionario médico
Ataxia — For other uses, see Ataxia (disambiguation). Ataxia (from Greek α [used as a negative prefix] + τάξις [order], meaning lack of order ) is a neurological sign and symptom that consists of gross lack of coordination of muscle movements. Ataxia is a … Wikipedia
Ataxia (genus) — Taxobox | name = Ataxia regnum = Animalia phylum = Arthropoda classis = Insecta ordo = Coleoptera familia = Cerambycidae subfamilia = Lamiinae genus = Ataxia genus authority = Haldeman, 1847 [ITIS|ID=701780|taxon= Ataxia ] subdivision ranks =… … Wikipedia
Ataxia — Wobbliness. Ataxia is incoordination and unsteadiness due to the brain’s failure to regulate the body’s posture and regulate the strength and direction of limb movements. Ataxia is usually a consequence of disease in the brain,… … Medical dictionary
Central pontine myelinosis — Infobox Disease Name = Central pontine myelinosis Caption = DiseasesDB = 2198 ICD10 = ICD10|G|37|2|g|35 ICD9 = ICD9|341.8 ICDO = OMIM = MedlinePlus = 000775 eMedicineSubj = neuro eMedicineTopic = 50 MeshID = D017590 Central pontine myelinolysis… … Wikipedia
ataxia — noun Etymology: Greek, from a + tassein to put in order Date: 1670 an inability to coordinate voluntary muscular movements that is symptomatic of some central nervous system disorders and injuries and not due to muscle weakness called also… … New Collegiate Dictionary
Spinocerebellar ataxia — (SCA) is a genetic disease with multiple types, each of which could be considered a disease in its own right. ymptomsSpinocerebellar ataxia (SCA) is one of a group of genetic disorders characterized by slowly progressive incoordination of gait… … Wikipedia
Cerebellar ataxia — Classification and external resources ICD 10 G11.1 G11.3 ICD 9 … Wikipedia
Spinocerebellar ataxia type-13 — (SCA13) is a rare autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, nystagmus, and ataxia of gait, stance and the limbs due to cerebellar dysfunction. Patients with SCA13 also tend to present with… … Wikipedia
