X连锁少汗性外胚层发育不良1家系EDA基因新突变

doi:10.35541/cjd.20230049

Chinese Journal of Dermatology ›› 2024, Vol. 57 ›› Issue (3): 262-264.doi: 10.35541/cjd.20230049

• Case Reports • Previous Articles Next Articles

A family with X-linked hypohidrotic ectodermal dysplasia caused by a new mutation in the EDA gene

Li Meizhao, Wu Wei, Luo Zhiqiang, Wang Fengjuan, Zhou Shuwen, Zhou Haiyuan, Shi Jianqiang

Department of Dermatology and Venereology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, Guangdong, China

Received:2023-01-31 Revised:2023-07-31 Online:2024-03-15 Published:2024-03-04
Contact: Wu Wei E-mail:wuwei1350187@126.com
Supported by:
National Natural Science Foundation of China（81872532）

Abstract

Li Meizhao, Wu Wei, Luo Zhiqiang, Wang Fengjuan, Zhou Shuwen, Zhou Haiyuan, Shi Jianqiang. A family with X-linked hypohidrotic ectodermal dysplasia caused by a new mutation in the EDA gene[J]. Chinese Journal of Dermatology, 2024, 57(3): 262-264.doi:10.35541/cjd.20230049

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［7］	Piletta PA, Calza AM, Masouyé I, et al. Hypohidrotic ectodermal dysplasia with recurrent otitis and sebaceous gland hypertrophy of the face［J］. Dermatology, 1995,191（4）:355⁃358. doi: 10.1159/000246601.
［8］	Orge C, Bonsmann G, Hamm H. Multiple sebaceous gland hyperplasias in X chromosome hypohidrotic ectodermal dysplasia［J］. Hautarzt, 1991,42（10）:645⁃647.

A family with X-linked hypohidrotic ectodermal dysplasia caused by a new mutation in the EDA gene

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