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[智力迟钝、惊厥与脑萎缩;毛囊角化病的主要神经学改变]

[Mental retardation convulsions and cerebral atrophy; main neurological changes in Darier's disease].

作者信息

López-Hernández A, Tamayo de Malo L, Cuéllar Alvarenga R

出版信息

Bol Med Hosp Infant Mex. 1980 May-Jun;37(3):531-7.

PMID:7397029
Abstract

Darier's disease is determined by an autosomal dominant gene and is clinically characterized by confluent hyperkarotic papules. Mental retardation may appear in up to 10-20% of patients. Convulsions, spinocerebellar tract degeneration, polyneuropathy, psychiatric disorders and cerebral atrophy occur with a low and as yet not precisely determined incidence. In the medical literature reviewed only two previous cases of cerebral atrophy associated with Darier's disease were found. This study describes six members of a family affected with an unusually high incidence of neurologic manifestations. The mother and her five sons showed skin lesions, which, on histological examination, revealed the characteristic pathological changes of Darier's disease. Two of the five siblings with convulsions and mental retardation underwent computed tomography of the brain and both patients revealed the classic findings in atrophy; moderate enlargement of the lateral ventricles and widening of the cortical sulci. Cerebral atrophy was correlated with mental retardation and convulsions.

摘要

Darier病由常染色体显性基因决定,临床特征为融合性角化过度丘疹。高达10% - 20%的患者可能出现智力发育迟缓。惊厥、脊髓小脑束变性、多发性神经病、精神障碍和脑萎缩的发生率较低且尚未精确确定。在查阅的医学文献中,仅发现两例与Darier病相关的脑萎缩病例。本研究描述了一个家族中的六名成员,他们出现神经系统表现的发生率异常高。母亲及其五个儿子均有皮肤损害,组织学检查显示具有Darier病的特征性病理变化。五名有惊厥和智力发育迟缓的兄弟姐妹中有两人接受了脑部计算机断层扫描,两名患者均显示出萎缩的典型表现;侧脑室中度扩大和脑沟增宽。脑萎缩与智力发育迟缓和惊厥相关。

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