Results 91 to 100 of about 282,297 (205)
Hereditary palmoplantar keratoderma - a focus on clinical and molecular genetic aspects.
, 2015 Hereditary palmoplantar keratoderma comprises a heterogenous group of genodermatoses. The clinical spectrum of palmoplantar keratoderma can range from pure skin thickening, restricted to palmoplantar skin to complex conditions with dental anomalies, eye ...
Kamaleswaran, Shailajah +3 more
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PATHOPHYSIOLOGY OF THE CYCLICAL EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (EPPK) IN THE KERATIN 9 MOUSE MODEL [PDF]
, 2017 Keratin 9 (KRT9/Krt9) is a type I intermediate filament protein that is constitutively expressed in the suprabasal layer of the thicker and specialized epidermis of the palmoplantar skin. Mutations at the KRT9/Krt9 locus cause epidermolytic palmoplantar
Shen, Joseph YuHung
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Mutation analysis of the KRT9 gene in a family with epidermolytic palmoplantar keratoderma
, 2023 Objective To investigate the pedigree and gene mutation of a family of patient with epidermolytic palmoplantar keratoderma (EPPK). Methods Clinical data were collected, and DNA samples were extracted from affected individuals and her parents. Whole-exome
Fang YANG +3 more
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Clinical Study on Palmoplantar Keratoderma [PDF]
, 2012 INTRODUCTION : Palmoplantar keratodermas are a heterogenous group of disorders characterized by hyperkeratosis of palms and soles. They may be inherited or acquired disorders.
Mohanasundari, P S
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, 2002 In 1901, Hans Voerner observed a family with a diffuse non-transgredient palmoplantar keratoderma of autosomal dominant inheritance. Histopathologically, he found epidermolytic hyperkeratosis as a characteristic sign and diagnostic criterion of this ...
Reis, A., Kuester, W., Hennies, H.C.
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Detection of gene mutation in a case of Nagashima-type palmoplantar keratoderma
Pifu-xingbing zhenliaoxue zazhi[Objective] To report a case of Nagashima-type palmoplantar keratoderma (NPPK), identify pathogenic gene, and assist clinical diagnosis and classification of this disease. [Methods] Clinical data of the patient were collected.
CAO Yuanyuan +5 more
doaj +1 more source
, 2004 BACKGROUND: Striated palmoplantar keratoderma or Brunauer-Fohs-Siemens syndrome is a very rare, focal, nonepidermolytic palmoplantar keratoderma with autosomal inheritance.
BIAGIOLI M. +4 more
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Isolated hereditary diffuse palmoplantar keratoderma in Hong Kong Chinese patients: a case series [PDF]
Hong Kong Medical Journal, 2021 P T, Yu +4 more
openaire +2 more sources
Hereditary palmoplantar keratoderma - a focus on clinical and molecular genetic aspects.
, 2014 Hereditary palmoplantar keratoderma comprises a heterogenous group of genodermatoses. The clinical spectrum of palmoplantar keratoderma can range from pure skin thickening, restricted to palmoplantar skin to complex conditions with dental anomalies, eye ...
Kamaleswaran, Shailajah +3 more
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Malignant melanoma in association with palmoplantar keratoderma
, 1999 A case of malignant melanoma arising on the hyperkeratotic little finger of a 46-year-old patient with palmoplantar keratoderma is reported. A pigmented lesion had been present since childhood, over a period of two years it became larger and darker and ...
Aygit, AC, Bayçin, HN, Demiralay, A
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