麦卡德尔病综述
McArdle's disease: a review.
作者信息
Lubran M M
出版信息
Ann Clin Lab Sci. 1975 Mar-Apr;5(2):115-22.
PMID:1092247
Abstract
The clinical features of McArdle's disease (inherited deficiency of skeletal muscle phosphorylase) and the histological and biochemical changes are described. Their possible causes are discussed in the light of recent knowledge of the biochemistry of muscular contraction. Diagnostic tests are detailed. Attention is drawn to the possibility that the disease may be due to primary defect of motoneurons.
摘要
描述了麦克尔迪氏病（骨骼肌磷酸化酶遗传性缺乏）的临床特征以及组织学和生化变化。根据肌肉收缩生物化学的最新知识，讨论了其可能的病因。详细介绍了诊断测试。提请注意该病可能是由于运动神经元原发性缺陷所致的可能性。
相似文献
1
McArdle's disease: a review.
Ann Clin Lab Sci. 1975 Mar-Apr;5(2):115-22.
2
[Apropos of a further case of absence of phosphorylase in the striated muscle (McArdle's disease)].
Rev Neurol (Paris). 1967 Feb;116(2):119-40.
3
[McArdle's metabolic myopathy].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1974;74(10):1485-90.
4
McArdle's syndrome (myophosphorylase deficiency). A study of a family.
Q J Med. 1967 Oct;36(144):565-78.
5
[McArdle's disease].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1969;69(11):1668-72.
6
Myopathy resembling McArdle's syndrome.
Arch Neurol. 1969 Jun;20(6):586-98. doi: 10.1001/archneur.1969.00480120032002.
7
[McArdle's syndrome].
Zh Nevropatol Psikhiatr Im S S Korsakova. 1973;73(6):820-5.
8
[Myasthenic form of a metabolic myopathy with dystrophic changes due to storage and symptoms resembling McArdle's syndrome (a case report)].
Psychiatr Neurol Med Psychol (Leipz). 1971 Nov;23(11):650-7.
9
Acute renal failure in McArdle's disease. Report of two cases.
N Engl J Med. 1972 Jun 8;286(23):1237-41. doi: 10.1056/NEJM197206082862304.
10
[A case of McArdle type myopathy. (Clinical observation, biochemical data, histopathological and ultrastructural findings)].
Rev Neurol (Paris). 1967 Nov;117(5):650-62.
Zotero 插件