Results 101 to 110 of about 282,297 (205)
Hereditary Painful Callosities Treated with L5 and S1 Pulsed Radiofrequency, Case Report
International Journal of PainHereditary palmoplantar Keratoderma (PPK) varies in presentation, where palm and sole lesions can be diffuse, focal or punctate. There is no specific curative treatment for hereditary PPK, and the resulting pain may significantly strain all aspects of ...
Moustafa Moustafa +2 more
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Diffuse palmoplantar keratoderma associated with acrocyanosis. A family study.
Acta dermato-venereologica, 1989 Four members of a family, in which 8 suffered from diffuse palmoplantar keratoderma associated with an uncommon form of acrocyanosis, are reported. Acrocyanosis and palmoplantar keratoderma do not always occur together and, therefore, an autosomal dominant inheritance for this association is suggested.
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Asian Journal of Medical SciencesBackground: Changes in skin, hair, and nails may be initial manifestations of an underlying thyroid hormone deficiency. Symptomatic treatment of cutaneous manifestations without treatment of underlying hypothyroidism contributes to long-term morbidity in
Swastika Debbarma , Aniruddha Ghosh
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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 +4 more
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Mutations in AAGAB underlie autosomal dominant punctate palmoplantar keratoderma
, 2017 Punctate palmoplantar keratoderma type 1 (PPPK1) is a rare autosomal dominant inherited skin disease, characterized by multiple hyperkeratotic lesions on the palms and soles. The causative gene for PPPK1 has been identified as AAGAB, which encodes α- and
J. McGrath +9 more
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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
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, 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 +3 more
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Pundate palmoplantar keratoderma (Brauer-Buschke-Fischer syndrome)
, 2007 Punctate palmoplantar keratoderma (PPPK) is a rare entity with an estimated prevalence rate of about 1.17 per 100 000. The exact etiology of the disorder is not known but a dual influence of genetic and environmental factors may trigger the disease.
Artuz, Ferda +6 more
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