congenital absence the skin
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Bart syndrome is a genetic disorder characterized by the association of congenital localized absence of skin, epidermolysis bullosa, lesions of the mouth mucosa, and dystrophic nails.
一种遗传疾病，以先天性局部皮肤缺损、大疱性表皮松解症、口腔粘膜病变、甲营养不良为特征。
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