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神经皮肤疾病的遗传学方面。

Genetic aspects of neurocutaneous disorders.

作者信息

Jentarra Garilyn, Snyder Shannon L, Narayanan Vinodh

机构信息

Children's Health Center, St. Joseph's Hospital and Medical Center, Barrow Neurological Institute, Phoenix, AZ, USA.

出版信息

Semin Pediatr Neurol. 2006 Mar;13(1):43-7. doi: 10.1016/j.spen.2006.01.010.

Abstract

Among the conditions that are included under the heading of "neurocutaneous disorders" are neurofibromatosis 1, tuberous sclerosis complex, von Hippel-Lindau, incontinentia pigmenti, Sturge-Weber syndrome, hypomelanosis of Ito, and linear nevus sebaceous syndromes. The clinical features, pathogenesis, and neurobiological basis of some of these disorders are discussed in other articles in this issue. We will focus on genetic aspects of a selected subgroup of these conditions, concentrating on the genetic defect, mutation spectrum, clinical genetic testing, and issues pertinent to counseling.

摘要

“神经皮肤疾病”这一标题下包含的病症有神经纤维瘤病1型、结节性硬化症复合体、冯·希佩尔-林道病、色素失禁症、斯特奇-韦伯综合征、伊藤色素减退症和线状皮脂腺痣综合征。本期其他文章讨论了其中一些病症的临床特征、发病机制和神经生物学基础。我们将重点关注这些病症中一个选定亚组的遗传学方面,集中探讨基因缺陷、突变谱、临床基因检测以及与遗传咨询相关的问题。

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