- A Case of Erythrokeratodermia Variabilis in Korean
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Oh DY, Jung KE, Lee JS, Koo DW
- KMID: 2456677
- Ann Dermatol.
- 2019 Aug;31(Suppl):S49-S51.
- doi: 10.5021/ad.2019.31.S.S49
No abstract available. -
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- A Case of Erythrokeratodermia Variabilis in Korean
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Oh DY, Jung KE, Lee JS, Koo DW
- KMID: 2456650
- Ann Dermatol.
- 2019 Aug;31(Suppl 1):S49-S51.
- doi: 10.5021/ad.2019.31.S.S49
No abstract available. -
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- Erythrokeratodermia Variabilis with Alopecia Universalis
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Lee JS, Sung YH, Lee JH, Park JK
- KMID: 2362051
- Ann Dermatol.
- 1990 Jan;2(1):17-20.
- doi: 10.5021/ad.1990.2.1.17
We describe a 8-year-old girl with erythrokeratodermia varibilis (EKV). This diagnosis was supported by erythematous, configurate patches over the entire body. Their size, shape and location varyed with enviromental factors and... -
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- Erythrokeratodermia Variabilis with Congenital Deaf-Mutism
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Nam HM, Kim UK, Park K, Park SD
- KMID: 2247598
- Korean J Dermatol.
- 2011 Apr;49(4):379-381.
Erythrokeratodermia variabilis is a rare genodermatosis characterized by the coexistence of randomly occurring, transient, erythematous patches and hyperkeratosis of the skin. A 25-year-old Uzbekistanian female with congenital deaf-mutism presented with... -
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- Erythrokeratodermia Variabilis Showing Gradual Disappearance of Erythema
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Kim H, Park IH, Kang JN, Seol JE, Sung HS
- KMID: 1802079
- Korean J Dermatol.
- 2014 Apr;52(4):260-263.
Erythrokeratodermia variabilis is an autosomal-dominant inherited disease associated with a mutation in gap junction beta (GJB) 3 and 4. It shows two characteristic features: migratory and irregularly shaped erythematous lesions... -
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