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Congenital Hypotrichosis, Eruptive Milia, and Palmoplantar Pits: A Case Report with Review of Literature

机译:先天性hyperrichosis,爆发性ilia和掌足坑:病例报告与文献综述。

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摘要

We report a ten-month-old male infant, presenting with congenital hypotrichosis of scalp, absence of eyebrows and eyelashes. He also had multiple milia over face and extremities along with palmoplantar pits. The infant was born to third degree consanguineous marriage. None of the family members had similar disease. Histopathology was consistent with milia. Based on these findings, a diagnosis of unclassified ectodermal dysplasia was made.
机译:我们报告了一个十个月大的男婴,表现为先天性头皮下垂症,没有眉毛和睫毛。他的面部和四肢也有多个m骨以及掌plant凹坑。婴儿出生于近亲三级婚姻。没有一个家庭成员患有类似疾病。组织病理学与纤毛一致。基于这些发现,对未分类的外胚层发育不良进行了诊断。

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