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骨发育异常性皮肤异色症:组织学特征及基于面板的外显子组测序在诊断中的作用

Geroderma osteodysplasticum: Histological features and the role of panel-based exome sequencing in diagnosis.

作者信息

Jewell Rosalyn, Brewer Paul, Stenton Sophie, Berry Ian R, Chatfield Sue, Fernandes James A, Peres Cesar, Wagner Bart E, Bennett Christopher

机构信息

a Yorkshire Regional Genetics Service , Chapel Allerton Hospital, Leeds Teaching Hospitals NHS Trust , Leeds , UK.

b Department of Orthopaedics , Sheffield Children's Hospital , Sheffield , UK.

出版信息

Ultrastruct Pathol. 2018 Mar-Apr;42(2):91-96. doi: 10.1080/01913123.2018.1427166. Epub 2018 Feb 9.

Abstract

Geroderma osteodysplasticum (GO) has clinical and histological features that overlap with other causes of wrinkly skin. Here we present the case of a child diagnosed with GO following exome sequencing of a panel of genes covering the wide differential diagnosis. The histological features of the overlapping conditions are presented, highlighting the utility of panel testing for conditions of this type. This is relevant to many genetic conditions and can influence ongoing management as exemplified by this case.

摘要

骨发育异常性皮肤老化症(GO)具有与其他导致皮肤起皱的病因重叠的临床和组织学特征。在此,我们报告一例在对涵盖广泛鉴别诊断的一组基因进行外显子组测序后被诊断为GO的儿童病例。文中呈现了重叠病症的组织学特征,突出了针对此类病症进行组套检测的实用性。这与许多遗传病症相关,并且如本病例所示,会对后续治疗产生影响。

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