- autosomal dominant pure cerebellar ataxia
- 常染色体显性遗传小脑性共济失调
Medical Chinese dictionary (湘雅医学词典). 2013.
Medical Chinese dictionary (湘雅医学词典). 2013.
Episodic ataxia — (EA) is an autosomal dominant disorder characterized by sporadic bouts of ataxia (severe discoordination) with or without myokymia (continuous muscle movement). Ataxia can be provoked by stress, startle, or heavy exertion such as exercise.… … Wikipedia
Cav2.1 — The Cav2.1 P/Q voltage dependent calcium channel is encoded by the gene|CACNA1A gene.Voltage dependent calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium dependent processes,… … Wikipedia
List of diseases (C) — A list of diseases in the English wikipedia.C* C syndrome * C1 esterase deficiency (angioedema)CaCac Cal* Cacchi Ricci disease * CACH syndrome * Cafe au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… … Wikipedia
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
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
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
Ataxin 1 — Ataxin 1, also known as ATXN1, is a human gene.cite web | title = Entrez Gene: ATXN1 ataxin 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=6310| accessdate = ] PBB Summary section title = summary text =… … Wikipedia