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Vohwinkel syndrome: ichthyosiform variant in a family *

机译:Vohwinkel综合征:家庭鱼眼形变异*

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Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an autosomal dominant inheritance. In this report, the authors present a case of a four-year-old boy with diffuse scaling over his entire body and transgredient palmoplantar hyperkeratosis with some fissured areas. Family evaluation revealed that his mother and other family members were affected. Based on his clinical findings and on family history, the diagnosis of the ichthyotic Vohwinkel syndrome subtype, characterized by generalized ichthyosis and palmoplantar hyperkeratosis, was established.
机译:Vohwinkel综合征属于遗传性掌plant角化病,具有常染色体显性遗传。在本报告中,作者介绍了一个四岁男孩的情况,该男孩的全身遍布鳞屑,并且掌gr性掌trans过度角化病带有一些裂痕区域。家庭评估显示他的母亲和其他家庭成员受到了影响。基于他的临床发现和家族史,建立了以鱼鳞病和掌plant过度角化病为特征的鱼鳞病Vohwinkel综合征亚型的诊断。

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