- A case of Hereditary Epidermolytic Palmoplantar Keratoderma
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Kim SE, Oh CW
- KMID: 2303126
- Korean J Dermatol.
- 2002 Aug;40(8):972-974.
The hereditary epidermolytic palmoplantar keratoderma (Vorner"s kerato derma) is characterized by autosomal dominantly inherited, marked, symmetrical thickening of the palms and soles. The presence of epidermolytic hyperkeratosis in skin biopsy... -
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- A case of punctate palmoplantar keratoderma
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Kim HJ, Lee ES
- KMID: 2146479
- Korean J Dermatol.
- 2000 Dec;38(12):1679-1680.
Punctate palmoplantar keratoderma(PPK), also called Buschke-Fisher-Brauer disease, is an autosomal dominant disease with variable penetrance. Clinically there are multiple tiny punctate keratoses over the entire palmoplantar surfaces. Lesions are discrete... -
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- Malnutrition-induced Acquired Palmoplantar Keratoderma: A Case Report
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Yun JW, Woo Y, Kim M, Park HJ
- KMID: 2391169
- Korean J Dermatol.
- 2017 Aug;55(7):454-456.
Palmoplantar keratoderma is characterized clinically by excessive thickening of the skin and histologically by hyperkeratosis on the palms and soles. It can be classified based on inheritance patterns, causes, clinical... -
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- A Case of Palmoplantar Keratoderma Presenting as Multiple Cutaneous Horns
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Choi HM, Kim JB, Lee SY, Kim SM, Ko EJ, Ro BI, Cho HK
- KMID: 2437000
- Korean J Dermatol.
- 2018 Nov;56(9):562-564.
No abstract available. -
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- A Case of Costello Syndrome with Severe Palmoplantar Keratoderma
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Kim HJ, Kim WI, Lee WK, Kim GW, Kim HS, Kim BS, Kim MB, Ko HC
- KMID: 2465960
- Korean J Dermatol.
- 2019 Sep;57(8):496-497.
No abstract available. -
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- A Case of Epidermolytic Palmoplantar Keratoderma
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Kang SK, Roh KH, Chang SE, Choi JH, Sung KJ, Moon KC, Koh JK
- KMID: 1604679
- Korean J Dermatol.
- 2002 Apr;40(4):445-448.
Palmoplantar keratodermas are divided into autosomal dominant and autosomal recessive groups by the mode of transmission. The autosomal dominantly transmitted group is further divided into epidermolytic and nonepidermolytic types according... -
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- A Case of Punctate Palmoplantar Keratoderma
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Kim MY, Park HJ, Lee JY, Cho BK
- KMID: 2250837
- Korean J Dermatol.
- 2002 Jun;40(6):715-717.
Punctate palmoplantar keratoderma(PPK) is an autosomal dominantly transmitted disease with variable penetrance. Clinically there are multiple tiny punctate keratoses over the entire palmoplantar surfaces. Lesions are discrete and diffuse, and... -
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- A Sporadic Case of Punctate Palmoplantar Keratoderma
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Ahn BK, Chun SH, Lee WS
- KMID: 1977875
- Korean J Dermatol.
- 2003 Dec;41(12):1694-1696.
Punctate palmoplantar keratoderma(PPK) is a rare disease, characterized by small, hard hyperkeratotic papules which are irregularly distributed on the palms and soles. PPK is an autosomal dominant disease with variable... -
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- The Therapeutic Effect of Oral Aromatic Retinoid(Ro 10-9359) in Palmoplantar Keratoderma
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Lee JB, Kim SC, Lee SH, Lee SN
- KMID: 1678312
- Korean J Dermatol.
- 1981 Oct;19(5):614-623.
No abstract available. -
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- Acquired Punctate Palmoplantar Keratosis: A Case Series
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Lim J, Woo Y, Kim M, Oh ST, Park HJ
- KMID: 2436650
- Korean J Dermatol.
- 2018 Feb;56(2):126-129.
Palmoplantar keratodermas (PPKs) are characterized by a thickening of the skin on the palms and soles of the feet caused by excessive keratin. Four forms can be seen, including diffuse,... -
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- A Case of Hereditary Epidermolytic Palmoplantar Keratoderma in Four Consecutive Generations
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Park SW, Hwang SW, Kim JW, Wang HY
- KMID: 2251094
- Korean J Dermatol.
- 2001 Feb;39(2):231-234.
We observed a family with 12 members in four consecutive generations affected by hereditary epidermolytic palmoplantar keratoderma(HEPPK). The affected family members demonstrated not only autosomal dominant inheritance, but also a... -
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- Familial Pityriasis Rubra Pilaris in Siblings
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Woo SH, Park SW, Kwak HB, Park SK, Yun SK, Kim HU, Park J
- KMID: 2440730
- Korean J Dermatol.
- 2019 Feb;57(2):97-98.
No abstract available. -
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- Hereditary Palmoplantar Keratoderma and Deafness Resulting from Genetic Mutation of Connexin 26
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Lee JY, In SI, Kim HJ, Jeong SY, Choung YH, Kim YC
- KMID: 2157865
- J Korean Med Sci.
- 2010 Oct;25(10):1539-1542.
- doi: 10.3346/jkms.2010.25.10.1539
Gap junctions, which mediate rapid intercellular communication, consist of connexins, small transmembrane proteins that belong to a large family of proteins found throughout the species. Mutations in the GJB2 gene,... -
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- The study of pathogenesis of palmoplantar keratoderma
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Bang D, Lee SH, Lee HS, Shim W
- KMID: 2303620
- Korean J Dermatol.
- 1991 Jun;29(3):337-345.
We investigated the biochemiesl change of keratin by the methods of SDS-PAGE and Two-dimensional gel electrophoresis, and observed electron microscopic ultrestructural changes in five Unna-Thost palmoplantar keratoderma patients and two... -
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- Comparison of Local Bath-PUVA with Steroid Treatment in Palmoplantar Pustular Psoriasis and Dyshidrotic Eczema
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Kim J, Choi YW, Choi HY, Myung KB
- KMID: 1568197
- Korean J Dermatol.
- 2000 Jun;38(6):742-749.
BACKGROUND: Local bath-PUVA(LB-PUVA) therapy has been recently tried for the treatment of palmoplantar pustular psoriasis and chronic eczema with successful results. However it has not been reported that the effectiveness... -
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- A Sporadic Case of Mal de Meleda Caused by Gene Mutation in SLURP-1 in Korea
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Oh YJ, Lee HE, Ko JY, Ro YS, Yu HJ
- KMID: 2171939
- Ann Dermatol.
- 2011 Aug;23(3):396-399.
- doi: 10.5021/ad.2011.23.3.396
Mal de Meleda (MDM), also known as keratoderma palmoplantaris transgrediens, is a rare inherited form of palmoplantar keratoderma. It is characterized by erythema and hyperkeratosis of the palms and soles,... -
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- A Clinicopathological Study of Palmoplantar Dermatoses
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Kang BS, Lee JD, Cho SH
- KMID: 2248955
- Korean J Dermatol.
- 2006 Jun;44(6):714-720.
BACKGROUND: Palmoplantar dermatoses have frequently been encountered in the dermatologic field. Many previous studies have focused on the specific diseases of palmoplantar dermatoses; however, none of them have included a... -
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- Two Familial Cases of Acrokeratoelastoidosis of Costa with Autosomal Dominant Inheritance
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Ham SH, Ha SJ, Park YM, Cho SH, Cho BK
- KMID: 2303444
- Korean J Dermatol.
- 1998 Oct;36(5):946-949.
Acrokeratoelastoidosis of Costa is a rare palmoplantar keratoderma with autosomal dominant inheritance. It is clinically charaeterized by small, firm, yellowish, shiny, translucent papules occumng over the dorsal hands, the knuckles,... -
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- Acral Erythema and Hyperpigmentation Induced by Tegafur
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Ha SJ, Ham SH, Park YM, Cho SH, Cho BK
- KMID: 2230591
- Korean J Dermatol.
- 1998 Apr;36(2):363-366.
Tegafur is a fluoropyrimidine structurally similar to 5-fluorouracil, used in the treatment of advanced gastrointestinal neoplasms. Mucocutaneous side reactions induced by this agent are rare and include photosensitivity of lichenoid... -
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- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in TRPV3 Gene
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Choi JY, Kim SE, Lee SE, Kim SC
- KMID: 2418801
- Yonsei Med J.
- 2018 Mar;59(2):341-344.
- doi: 10.3349/ymj.2018.59.2.341
Olmsted syndrome (OS) is a rare congenital skin disorder characterized by severe palmoplantar and periorificial keratoderma, alopecia, onychodystrophy, and severe pruritus. Recently, pathogenic ‘gain-of-function‘ mutations of the transient receptor potential... -
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