8A02.12
与遗传变性性疾患相关的肌张力障碍
Dystonia associated with heredodegenerative disorders
- 上级条目
- 8A02.1 继发性肌张力障碍
- 层级
- 5 级
定义
肌张力障碍作为更复杂的遗传性神经退化性疾病的一部分发生。它不是单纯的肌张力障碍，可能会出现其他神经系统表现，如共济失调、锥体征和认知问题。
Dystonia occurring as a part of a more complex heredodegenerative disorder. It is not a pure dystonia and other neurological findings such as ataxia, pyramidal signs and cognitive issues may be seen.
索引词 可用于检索该条目的同义词与别名
- 与遗传变性性疾患相关的肌张力障碍
- 常染色体显性遗传疾患引起的肌张力障碍
- 快发病性肌张力障碍-帕金森综合征
- 快发病性肌张力障碍-帕金森综合征
- 齿状核红核苍白球路易体萎缩引起的肌张力障碍
- 齿状核红核苍白球丘脑下核萎缩引起的肌张力障碍
- 亨廷顿病引起的肌张力障碍
- 常染色体隐性遗传疾患引起的肌张力障碍
- 威尔逊病引起的及张力障碍
- C型尼曼氏病引起的肌张力障碍
- 其他常染色体隐性遗传代谢障碍引起的肌张力障碍
- GM2神经节苷脂贮积病引起的肌张力障碍
- 异染性脑白质营养不良引起的肌张力障碍
- 同型胱氨酸尿症引起的肌张力障碍
- 戊二酸血症引起的肌张力障碍
- Hartnup病引起的肌张力障碍
- 哈特纳普病引起的肌张力障碍
- 共济失调-毛细血管扩张症引起的肌张力障碍
- 脑组织铁沉积神经变性病1型引起的肌张力障碍
- 脑内铁沉积神经变性病引起的肌张力障碍
- 包括Parkin突变的青少年型帕金森病引起的肌张力障碍
- 可能为常染色体隐性遗传的肌张力障碍
- 进行性苍白球变性
- X连锁显性遗传疾患引起的肌张力障碍
- Rett综合征引起的肌张力障碍
- 雷特氏综合征引起的肌张力障碍
- X连锁隐性遗传疾患引起的肌张力障碍
- 耳聋-肌张力障碍-视神经萎缩综合征
- Mohr-Tranebjærg综合征
- 莫-特综合征
- Pelizaeus-Merzbache病引起的肌张力障碍
- 佩利措伊斯-梅茨巴赫病引起的肌张力障碍
- Lesch-Nyhan综合征引起的肌张力障碍
- 莱施-奈恩综合征引起的肌张力障碍
- 线粒体细胞病引起的肌张力障碍
- Leber病引起的肌张力障碍
- 利伯氏病引起的肌张力障碍
- 其他线粒体细胞病引起的肌张力障碍
- 变异遗传的肌张力障碍
- 家族性基底神经节钙化引起的肌张力障碍
- 某些特指的遗传性疾患引起的肌张力障碍
- 与家族性基底神经节钙化相关的肌张力障碍
- 孤立性遗传性维生素E缺乏引起的肌张力障碍
- 遗传性痉挛性截瘫引起的肌张力障碍
- 肌张力障碍16型
- 婴儿肌张力障碍-帕金森病
英文词条（37）
- Dystonia associated with heredodegenerative disorders
- Dystonia due to autosomal dominant disorders
- Rapid-onset dystonia-parkinsonism
- Dystonia due to dentatorubropallidoluysian atrophy
- Dystonia due to Huntington disease
- Dystonia due to autosomal recessive disorders
- Dystonia due to Wilson disease
- Dystonia due to Niemann-Pick disease type C
- Dystonia due to other autosomal recessive metabolic disorders
- Dystonia due to GM2 gangliosidosis
- Dystonia due to Metachromatic leukodystrophy
- Dystonia due to homocystinuria
- Dystonia due to glutaric acidaemia
- Dystonia due to Hartnup disease
- Dystonia due to ataxia-telangiectasia
- Dystonia in neurodegeneration with brain iron accumulation type 1
- Dystonia due to Juvenile Parkinson Disease including Parkin mutation
- Probable autosomal recessive dystonia
- Progressive pallidal degeneration
- Dystonia due to X-linked dominant disorders
- Dystonia due to Rett syndrome
- Dystonia due to X-linked recessive disorders
- Deafness-dystonia optic atrophy syndrome
- Mohr-Tranebjærg syndrome
- Dystonia due to Pelizaeus-Merzbacher disease
- Dystonia due to Lesch-Nyhan syndrome
- Dystonia due to mitochondrial cytopathies
- Dystonia due to Leber's disease
- Dystonia due to other mitochondrial cytopathies
- Dystonia of variable inheritance
- Dystonia due to Familial basal ganglia calcifications
- Dystonia due to certain specified inherited disorders
- Dystonia associated with familial basal ganglia calcifications
- Dystonia due to isolated hereditary vitamin E deficiency
- Dystonia due to hereditary spastic paraplegia
- Dystonia 16
- Infantile dystonia-parkinsonism
后组配轴 Postcoordination
后组配是在主干编码之后追加的可选扩展轴（如侧别、具体解剖部位、严重程度），用于把「部位 + 侧别 + 病程」等细节一次表达完整。只有标注「必填」的轴在组合编码时必须给出，其余可留空。
- 临床表现hasManifestation可选