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Wolcott-Rallison Syndrome

机译:Wolcott-Rallison综合征

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Multiple epiphyseal dysplasia with early-onset diabetes mellitus (also known as Wolcott-Rallison syndrome) is a rare autosomal recessive disorder that manifests itself in early infancy with symptoms of diabetes mellitus. Short stature and walking difficulties become evident in the 2 nd year of life when the child starts to walk. These skeletal changes are progressive with age. There is usually a short trunk, excessive lordosis, a short and broad chest, and genu valgum. This report presents a case of Wolcott-Rallison syndrome in a 10 year old child.
机译:患有早发性糖尿病的多发性骨phy发育不良(也称为沃尔科特-罗利森综合征)是一种罕见的常染色体隐性遗传疾病,表现为婴儿早期并伴有糖尿病症状。在孩子开始走路的第二个 年,矮小的身材和行走困难就变得很明显。这些骨骼变化随着年龄的增长而逐渐发展。通常有一个短的躯干,过度的脊柱前凸,一个短而宽的胸部以及外阴外翻。该报告介绍了一名10岁儿童的沃尔科特·罗里森综合症。

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