脑巨人症。

A. Poznanski, G. Manson, R. Mellinger, J. Stephenson
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引用次数: 0

摘要

据报道,研究中有10名儿童的身体发现,此前报道的病例被归类为脑巨人症。这些发现包括智力迟钝;超前的身高、体重和骨龄;还有一种特有的相。6例有气脑造影,均显示通讯性脑积水。核图正常。尿17-KS类固醇排泄随年龄增加,但水平与生理年龄相符。肾上腺对地塞米松抑制和给药的反应正常。这种情况被认为是先天性中枢神经系统功能障碍、智力低下和下丘脑对垂体前叶功能控制改变的反映。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebral gigantism.
Studies are reported of 10 children having physical findings previously reported in cases classified as showing cerebral gigantism. These findings included mental retardation; advanced height, weight, and bone age; and a characteristic facies. Six had pneumoencephalography and all showed communicating hydrocephalus. Karyograms were normal. Urinary 17-KS steroid excretion was increased for chronologic age, but levels were compatible with physiologic age. Adrenal response to dexamethasone suppression and metyrapone administration was normal. The condition is regarded as a reflection of congenital central nervous system dysfunction with mental retardation and altered hypothalamic control of anterior pituitary function.
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