- ataxias
- a·tax·i·a || ə'tæksɪə n. inability to coordinate muscular movement
English contemporary dictionary. 2014.
ataxias
Look at other dictionaries:
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
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
Hyperkinesia — This article is about hyperkinesia, the pathologically increased muscular movement. For hyperkinesis, hyperactivity often seen in children, see Hyperkinesis. Hyperkinesia Basal ganglia and its normal pathways. This circuitry is often disrupted in … Wikipedia
Dysmetria — (Greek: difficult to measure ) refers to a lack of coordination of movement typified by the undershoot and/or overshoot of intended position with the hand, arm, leg, or eye. It is sometimes described as an inability to judge distance or… … Wikipedia
Ataxia de Friedreich — Saltar a navegación, búsqueda Ataxia de Friedreich Clasificación y recursos externos Aviso médico CIE 10 … Wikipedia Español
Hereditary spastic paraplegia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = ICD10 = ICD10|G|11|4|g|10 ICD9 = ICD9|334.1 ICDO = OMIM = MedlinePlus = eMedicineSubj = pmr eMedicineTopic = 45 MeshID = D015419 Hereditary Spastic Paraplegia (HSP), also called Familial… … Wikipedia
Purkinje cell — Infobox neuron neuron name = Purkinje cell image neuron = PurkinjeCell.jpg caption neuron = Drawing of pigeon Purkinje cells (A) by Santiago Ramon y Cajal location = Cerebellum function = inhibitory projection neuron neurotranmitter = GABA… … Wikipedia
Trinucleotide repeat disorder — Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation … Wikipedia
Spinocerebellar ataxia type-6 — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 12339 ICD10 = ICD10|G|11|2|g|10 ICD9 = ICD9|334.9 ICDO = OMIM = 183086 MedlinePlus = eMedicineSubj = neuro eMedicineTopic = 556 Spinocerebellar ataxia type 6 (SCA6) is a rare, late onset,… … Wikipedia
ATXN2 — Ataxin 2, also known as ATXN2, is a human gene. PBB Summary section title = summary text = Mutations in ATXN2 cause spinocerebellar ataxia type 2 (SCA2). The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of… … Wikipedia
