An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases-Reference-Cited by-同舟云学术

An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases

Published:2021-12-13 Issue: Volume: Page:
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Inazawa‐Terada Minako¹,Namiki Takeshi¹^ORCID,Omigawa Chika¹,Fujimoto Tomoko¹,Munetsugu Takichi¹,Ugajin Tsukasa¹,Shimomura Yutaka²^ORCID,Ohshima Yuichiro³,Yoshida Kazue⁴^ORCID,Niizeki Hironori⁴^ORCID,Hayashi Ryota⁵^ORCID,Nakano Hajime⁶,Yokozeki Hiroo¹^ORCID

Affiliation:

1. Department of Dermatology Graduate School of Medical and Dental Sciences Tokyo Medical and Dental University Tokyo Japan

2. Department of Dermatology Yamaguchi University Graduate School of Medicine Ube Japan

3. Department of Dermatology Aichi Medical University School of Medicine Nagakute Japan

4. Division of Dermatology National Center for Child Health and Development Tokyo Japan

5. Division of Dermatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan

6. Department of Dermatology Hirosaki University Graduate School of Medicine Hirosaki Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.16278

Reference27 articles.

1. HEREDITARY ECTODERMAL DYSPLASIA (CONGENITAL ECTODERMAL DEFECT)

2. X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

3. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

4. Gene defect in ectodermal dysplasia implicates a death domain adapter in development

5. Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus

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2. Rare Pediatric Genetic Case Report of X-linked Hypohidrotic Ectodermal Dysplasia Type 1;Cureus;2023-12-02

3. Extended Overview of Ocular Phenotype with Recent Advances in Hypohidrotic Ectodermal Dysplasia;Children;2022-09-06