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Hypohidrotic ectodermal dysplasia: A report of two cases.

作者信息

Miyake Tomomi, Kiniwa Yukiko, Kosho Tomoki, Nakano Hajime, Okuyama Ryuhei

机构信息

Departments of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan.

Departments of Medical Genetics, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

J Dermatol. 2017 Apr;44(4):479-481. doi: 10.1111/1346-8138.13479. Epub 2016 Jun 6.

DOI:10.1111/1346-8138.13479
PMID:27264909
Abstract
摘要

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[9]
Clinical, radiographic, and genetic characteristics of hypohidrotic ectodermal dysplasia: A cross-sectional study.

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引用本文的文献

[1]
Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia.

BMC Oral Health. 2024-1-27

[2]
No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.

Orphanet J Rare Dis. 2021-2-23

[3]
Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib.

Acta Derm Venereol. 2021-1-4

[4]
Pathogenic Mutations in Chinese Han Families With Hypohidrotic Ectodermal Dysplasia and Genotype-Phenotype: A Correlation Analysis.

Front Genet. 2020-2-4

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