Letter to the Editor
Case of X-linked hypohidrotic ectodermal dysplasia with a novel EDA missense mutation
Masahito Yasuda,
Corresponding Author
Masahito Yasuda
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Correspondence: Masahito Yasuda, M.D., Ph.D., Department of Dermatology, Gunma University Graduate School of Medicine, 3-39-22 Showa-Machi, Maebashi, Gunma 371-8511, Japan. Email:
[email protected]Search for more papers by this author Chikako Kishi,
Chikako Kishi
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Search for more papers by this author Yoko Yokoyama,
Yoko Yokoyama
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Search for more papers by this author Hiroo Amano,
Hiroo Amano
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Search for more papers by this author Osamu Ishikawa,
Osamu Ishikawa
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Search for more papers by this author
Masahito Yasuda,
Corresponding Author
Masahito Yasuda
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Correspondence: Masahito Yasuda, M.D., Ph.D., Department of Dermatology, Gunma University Graduate School of Medicine, 3-39-22 Showa-Machi, Maebashi, Gunma 371-8511, Japan. Email:
[email protected]Search for more papers by this author Chikako Kishi,
Chikako Kishi
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Search for more papers by this author Yoko Yokoyama,
Yoko Yokoyama
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Search for more papers by this author Hiroo Amano,
Hiroo Amano
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Search for more papers by this author Osamu Ishikawa,
Osamu Ishikawa
Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan
Search for more papers by this author
First published: 05 June 2015
No abstract is available for this article.
References
- 1Kere J, Srivastava AK, Montonen O et al. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet 1996; 13: 409–416.
- 2Gunadi, Miura K, Ohta M et al. Two novel mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia. Pediatr Res 2009; 65: 453–457.
- 3Koguchi-Yoshioka H, Wataya-Kaneda M, Yutani M et al. Atopic diathesis in hypohidrotic/anhidrotic ectodermal dysplasia. Acta Derm Venereol 2015; 95: 476–479.
- 4Dietz J, Kaercher T, Schneider AT et al. Early respiratory and ocular involvement in X-linked hypohidrotic ectodermal dysplasia. Eur J Pediatr 2013; 172: 1023–1031.
