Results 81 to 90 of about 27,969 (160)

Acral malignant melanoma and striated palmoplantar keratoderma (Brunauer-Fohs-Siemens syndrome): a fortuitous association?

, 2004
BACKGROUND: Striated palmoplantar keratoderma or Brunauer-Fohs-Siemens syndrome is a very rare, focal, nonepidermolytic palmoplantar keratoderma with autosomal inheritance.
BIAGIOLI M., POGGIALI S., FIMIANI M., CUCCIA A., RUBEGNI P.   +4 more
core   +1 more source

Clinical and genetic characterisation of palmoplantar keratoderma

Palmoplantar keratodermi er en tilstand kendetegnet ved hård og fortykket hud på håndflader og fodsåler. Ud over de ofte iøjnefaldende hudforandringer, kan sygdommen også ledsages af både smerter, sved- og lugtgener.
Gram, Stine Bjørn; id_orcid
core   +1 more source

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
core   +1 more source

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
core  

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, Bygum, Anette, Bach, Rasmus Overgaard, Ousager, Lilian Bomme   +3 more
core  

Palmoplantar keratoderma of Unna-Thost : response to biotin in one family

, 1992
Three members of a family with Unna-Thost palmoplantar keratoderma who showed skin improvement whilst receiving oral biotin are ...
R. Piccinno, F. Saleh, C. Corbetta, S. Menni, D. Melotti   +4 more
core   +1 more source

Towards characterization of palmoplantar keratoderma caused by gain-of-function mutation in loricrin: analysis of a family and review of the literature

, 2006
Loricrin keratoderma is an autosomal dominant palmoplantar keratoderma heterogeneous in clinical appearance. We report a family with diffuse ichthyosis and honeycomb palmoplantar keratoderma but no occurrence of pseudoainhums or autoamputations.
Traupe, H., Fischer, B., Tinschert, S., Hennies, Hans C., Gedicke, M.M., Hennies, H.C.   +5 more
core   +1 more source

Non-small-cell lung cancer with nonfamilial diffuse palmoplantar keratoderma

, 2002
Palmoplantar keratoderma (PPK) is a congenital or acquired disorder characterized by the abnormal thickening of the skin of the palms and soles. The thickening can present as a diffuse, focal or punctate pattern.
Kars, A, Altundag, O, Guler, N, Akdogan, A, Engin, H   +4 more
core  

Hypopigmentation-punctate palmoplantar keratoderma syndrome [PDF]

, 2020
openaire   +1 more source

Naxos Disease [PDF]

, 2005
Since 1995, according to the World Health Organisation’s classification of cardiomyopathies, Naxos disease has been considered as the recessive form of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C).1 It is a stereotype association of
Tsatsopoulou, Adalena, Nikos Protonotarios, Adalena Tsatsopoulou, Protonotarios, Nikos   +3 more
core