DISTRIBUTION OF AFFECTED NERVE CELLS IN A CASE OF AMYOTONIA CONGENITA
DISTRIBUTION OF AFFECTED NERVE CELLS IN A CASE OF AMYOTONIA CONGENITA
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先天性肌强直病例中受影响神经细胞的分布
DOI：
10.1001/archneurpsyc.1938.02270080121008
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发表时间：
1938
影响因子：
1.9
通讯作者：
J. L. Conel
中科院分区：
文献类型：
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作者：
J. L. Conel
马尔堡、1 Foot、2 Grinker 3等描述了先天性肌强直和Werdnig-Hoffmann病病例中受累细胞的一般外观。在儿童医院对一例这种罕见疾病进行的尸检使得对大脑和脊髓的所有部分进行研究成为可能。病例1的临床报告历史- 一名男童，生于1934年7月14日，因身体虚弱于11月13日入住婴儿医院。家族史很有趣，因为有九次怀孕。第二次和第三次妊娠终止于出生的孩子，他们分别活了11个月和9个月，死于肌肉无力和肺炎。第六、第七和第八次怀孕均以流产告终。患者足月正常出生。无明显产后并发症。孩子出生后进展良好，除了频繁的
The general appearance of affected cells in cases of amyotonia congenita and Werdnig-Hoffmann disease has been described by Marburg, 1 Foot, 2 Grinker 3 and others. An autopsy performed at the Children's Hospital in a case of this rare disease has made possible a study of all parts of the brain and spinal cord. CLINICAL REPORT OF CASE Case 1.— History. —A boy, born on July 14, 1934, was admitted to the Infants' Hospital on November 13 because of weakness. The family history was of interest in that there had been nine pregnancies. The second and third pregnancies terminated in the birth of children who lived eleven and nine months, respectively, and died of muscular weakness and pneumonia. The sixth, seventh and eighth pregnancies terminated in miscarriages. The patient was born normally at full term. There were no evident postnatal complications. The child progressed well after birth except for frequent