Results 201 to 210 of about 2,048 (238)
Polypoid cystitis with pachydermoperio-stosis: An unusual association
Indian Journal of Urology, 2000 Kanumury Ramesh +2 more
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Primary hypertrophic osteoarthropathy: phenotypic variability and penetrance rate in heterozygotes for <i>SLCO2A1</i> variants. [PDF]
JBMR PlusArcanjo AM +6 more
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International Journal of Rheumatic Diseases, 2023
Primary pachydermoperiostosis is a rare genetic disease affecting the skin and musculoskeletal system. In contrast to secondary hypertrophic osteoarthropathy, primary pachydermoperiostosis is considered a benign condition.
E. Rabhi +6 more
semanticscholar +1 more source
Primary pachydermoperiostosis is a rare genetic disease affecting the skin and musculoskeletal system. In contrast to secondary hypertrophic osteoarthropathy, primary pachydermoperiostosis is considered a benign condition.
E. Rabhi +6 more
semanticscholar +1 more source
Pachydermoperiostosis: an update
Clinical Genetics, 2005Pachydermoperiostosis (PDP) is a rare genodermatosis, characterized by pachydermia, digital clubbing, periostosis and an excess of affected males. Although an autosomal dominant model with incomplete penetrance and variable expression has been proved, both autosomal recessive and X‐linked inheritance have been suggested.
Lorenzo Sinibaldi +5 more
openaire +3 more sources
Myelofibrosis in a patient with pachydermoperiostosis
Clinical and Experimental Dermatology, 2005Pachydermoperiostosis (idiopathic or primary hypertrophic osteoarthropathy) is a rare condition of unknown origin involving the skin and the skeleton, with an autosomal dominant transmission. We report a case of anaemia in a patient with pachydermoperiostosis indicating myelofibrosis, and review the literature and the pathogenetic mechanisms.
C. Bachmeyer +3 more
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Acta Medica Scandinavica, 1970
Abstract. The report concerns pachydermoperiostosis in two women, mother and daughter, a relationship which has never before been noted. Another unusual aspect is that the characteristic features of the condition were noted already at the birth of the daughter. Moreover both have had symptoms of disturbed gonadal function.
openaire +2 more sources
Abstract. The report concerns pachydermoperiostosis in two women, mother and daughter, a relationship which has never before been noted. Another unusual aspect is that the characteristic features of the condition were noted already at the birth of the daughter. Moreover both have had symptoms of disturbed gonadal function.
openaire +2 more sources