Letter to the Editor
Hypohidrotic ectodermal dysplasia: A report of two cases
Tomomi Miyake,
Tomomi Miyake
Departments of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan
Search for more papers by this author Yukiko Kiniwa,
Corresponding Author
Yukiko Kiniwa
Departments of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan
Correspondence: Yukiko Kiniwa, M.D., Ph.D., Department of Dermatology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. Email:
[email protected]Search for more papers by this author Tomoki Kosho,
Tomoki Kosho
Departments of Medical Genetics, Shinshu University School of Medicine, Matsumoto, Japan
Search for more papers by this author Hajime Nakano,
Hajime Nakano
Department of Dermatology, Hirosaki University School of Medicine, Hirosaki, Japan
Search for more papers by this author Ryuhei Okuyama,
Ryuhei Okuyama
Departments of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan
Search for more papers by this author
Tomomi Miyake,
Tomomi Miyake
Departments of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan
Search for more papers by this author Yukiko Kiniwa,
Corresponding Author
Yukiko Kiniwa
Departments of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan
Correspondence: Yukiko Kiniwa, M.D., Ph.D., Department of Dermatology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan. Email:
[email protected]Search for more papers by this author Tomoki Kosho,
Tomoki Kosho
Departments of Medical Genetics, Shinshu University School of Medicine, Matsumoto, Japan
Search for more papers by this author Hajime Nakano,
Hajime Nakano
Department of Dermatology, Hirosaki University School of Medicine, Hirosaki, Japan
Search for more papers by this author Ryuhei Okuyama,
Ryuhei Okuyama
Departments of Dermatology, Shinshu University School of Medicine, Matsumoto, Japan
Search for more papers by this author
First published: 06 June 2016
No abstract is available for this article.
REFERENCES
- 1Itin PH, Fistarol SK. Ectodermal dysplasias. Am J Med Genet C Semin Med Genet 2004; 131C: 45–51.
- 2Burger K, Schneider AT, Wohlfart S et al. Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia. Am J Med Genet A 2014; 164A: 2424–2432.
- 3More CB, Bhavsar K, Joshi J et al. Hereditary ectodermal dysplasia: a retrospective study. J Nat Sci Biol Med 2013; 4: 445–450.
- 4Monreal AW, Zonana J, Ferguson B. Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations. Am J Hum Genet 1998; 63: 380–389.
- 5Hsu MM, Chao SC, Lu AC. A novel missense mutation (Gln306His) in exon 7 of the ED1 gene causing anhidrotic ectodermal dysplasia with prominent milia-like facial sebaceous papules. Br J Dermatol 2003; 149: 443–444.
