脑、脊髓受累 1.肌萎缩侧索硬化Amyotrophic LateralSclerosis 2. 肝豆状核变性HepatolenticularDegeneration(Wilson Disease) 3.多发性硬化Multiple Sclerosis 4. 视神经脊髓炎NeuromyelitisOptica. 5 . 脊髓延髓肌萎缩症(肯尼迪病)Spinal and BulbarMuscular Atrophy (Kennedy Disease) 6.脊髓性肌萎缩症SpinalMuscularAtrophy 7.脊髓小脑性共济失调SpinocerebellarAtaxia 脑受累 8.自身免疫性脑炎 AutoimmuneEncephalitis 9. 法布雷病Fabry Disease 10. 遗传性多发脑梗死性痴呆HereditaryMulti-infarctDementia (Cerebral Autosomal Dominant Arteriopathy withSubcortical Infarcts andLeukoencephalopathy, CADASLL) 11.亨廷顿舞蹈病HuntingtonDisease 12 . Leber遗传性视神经病变LeberHereditary Optic Neuropathy 13.枫糖尿症Maple Syrup UrineDisease 14. 甲基丙二酸血症MethylmalonicAcademia 15.线粒体脑肌病MitochodrialEncephalomyopathy 16.多系统萎缩Multiple SystemAtrophy 17.帕金森病(青年型、早发型)Parkinson Disease (Young-onset, Early-onset). 18.苯丙酮尿症Phenylketouria 19.原发性遗传性肌张力不全PrimaryHereditaryDystonia 20 .婴儿严重肌阵挛性癫痫(Dravet综合征)Severe Myoclonic Epilepsy In Infaricy (Dravet Syndrome) 21 .结节性硬化症TuberousSclerosisComplex 22 . x-连锁肾上腺脑白质营养不良X-linkedLdrenoleuko Dystrophy 周围神经、肌肉受累 23 . 原发性肉碱缺乏症CarnitineDeficiency. 24. 腓骨肌萎缩症Charcot-Marie-ToothDisease 25 . 先天性肌无力综合征CongenitalMyasthenic Syndrome 26. 先天性肌强直(非营养不良性肌强直综合征)Congenital Myotonia Syndrome(Non-Dystrophic Myotonia, NDM) 27 . 全身型重症肌无力General Myathenic Gravis 28. 戊二酸血症Ⅰ型GhutaricAcidemia Type Ⅰ 29 . 糖原累积病(Ⅰ型、Ⅱ型)GlycogenStorage Disease (Type Ⅰ. Ⅱ) 30. 长链3-羟酰基辅酶A脱氢酶缺乏症 Long Chain3-hydroxyacy-CoADehydrogenase Deficiency 31. 中链酰基辅酶A脱氢酶缺乏症Medium Chain Acyl-CoA DehydrogenaseDeficiency 32. 多灶性运动神经病Multi-FocalMotor Neurothy 33. 多种酰基辅酶A脱氧酶缺乏症Multiple Acyl-CoA DehydrogenaseDeficiency 34 . 肌强直性营养不良MvotonicDystrophy 35. POEMS综合征POEMS Syndrome 36. 卟啉病Porpbyria 37 .原发性轻链型淀粉样变PrimaryLight Chain Amyloidosis 38. 进行性肌营养不良ProgressiveMuscular Dystrophies 39 . 极长链酰基辅酶A脱氢酶缺乏症Very Long Chain Acyl-CoADehydrogenase Deficiency 39种疾病,一些脂肪酸代谢酶缺乏可以引起代谢性肌肉病加入神经系统疾病,多系统受累神经系统症状不突出未收入,希望各位老师指正。 编辑:伊万 |
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来自: zskyteacher > 《中枢神经系统》