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遗传性鱼鳞病:综合征型。

Inherited ichthyosis: Syndromic forms.

作者信息

Yoneda Kozo

机构信息

Department of Dermatology, Faculty of Medicine, Kagawa University, Kagawa, Japan.

出版信息

J Dermatol. 2016 Mar;43(3):252-63. doi: 10.1111/1346-8138.13284.

Abstract

Among diseases that cause ichthyosis as one of the symptoms, there are some diseases that induce abnormalities in organs other than the skin. Of these, diseases with characteristic signs are regarded as syndromes. Although these syndromes are very rare, Netherton syndrome, Sjögren-Larsson syndrome, Conradi-Hünermann-Happle syndrome, Dorfman-Chanarin syndrome, ichthyosis follicularis, atrichia and photophobia (IFAP) syndrome, and Refsum syndrome have been described in texts as representative ones. It is important to know the molecular genetics and pathomechanisms in order to establish an effective therapy and beneficial genetic counseling including a prenatal diagnosis.

摘要

在以鱼鳞病为症状之一的疾病中,有一些疾病会诱发皮肤以外器官的异常。其中,具有特征性体征的疾病被视为综合征。尽管这些综合征非常罕见,但Netherton综合征、Sjögren-Larsson综合征、Conradi-Hünermann-Happle综合征、Dorfman-Chanarin综合征、毛囊性鱼鳞病、脱毛和畏光(IFAP)综合征以及Refsum综合征在文献中被描述为代表性综合征。了解分子遗传学和发病机制对于建立有效的治疗方法以及提供包括产前诊断在内的有益遗传咨询非常重要。

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