Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report

Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report

ObjectiveTo report the clinical characteristics of a case of Autosomal recessive woolly hair/ hypotrichosis(ARWH/HT, OMIM:278150/604379) in a child, analyze and identify the causative gene and mutation site. A review of related research at home and abroad was conducted to summarize the current progr...

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Bibliographic Details
Main Authors: Ying Xie, Sha Luo, Yumei Yang, Xin Zou, Shuying Lv, Meijiao Du, Yonglong Xu, Xiaojuan Song, Changjie Qi, Nuo Li, Dingquan Yang
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-07-01
Series:Frontiers in Medicine
Subjects:
woolly hair
autosomal recessive
LIPH gene
mutation
case report
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2025.1563299/full
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https://www.frontiersin.org/articles/10.3389/fmed.2025.1563299/full

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