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[具有与遗传性脊髓小脑变性相似的复杂神经学特征的皮肤上皮瘤病家族型。关于4例病例,包括1例有解剖学 - 临床描述的病例]

[Familial form of cutaneous epitheliomatosis with complex neurological characteristics similar to hereditary spinocerebellar degeneration. Apropos of 4 cases including one case with anatomo-clinical description].

作者信息

Chateau R, Tommasi M, Groslambert R, Perret J, Pasquier B

出版信息

Rev Neurol (Paris). 1975 Jun;131(6):387-406.

PMID:1209055
Abstract

The authors report an observation in which four siblings were affected by both multiple cutaneous epitheliomatosis and complex but relatively stereotyped neurological disorders. Clinically, the main syndrome was cerebello-spinal ataxia with involvement of the anterior horns of the spinal cord with less marked pyramidal and extra-pyramidal features. Neuropathological examination of one of the cases revealed lesions of essentially cerebello-spinal degeneration suggestive of Menzel's disease. The possible connection between the neural and cutaneous lesions is discussed. All the various etiological categories possible have been ruled out; not one being entirely satisfactory, except for the very broad category of genetic neuro-dermatoses.

摘要

作者报告了一项观察结果,其中四个兄弟姐妹同时患有多发性皮肤上皮瘤病和复杂但相对刻板的神经疾病。临床上,主要综合征为小脑脊髓共济失调,累及脊髓前角,锥体束和锥体外系特征不明显。对其中一例进行的神经病理学检查显示,病变本质上为小脑脊髓变性,提示为门泽尔病。文中讨论了神经病变与皮肤病变之间可能的联系。所有可能的病因类别均已排除;除了非常宽泛的遗传性神经皮肤病类别外,没有一个类别能完全令人满意。

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