Results 71 to 80 of about 740 (177)
Alteration of Matrix Macromolecule Synthesis by Fibroblasts from a Patient with Pachydermoperiostosis [PDF]
, 1996 Pachydermoperiostosis (primary hypertrophic osteoarthropathy) is a very rare genetic disease characterized by pachydermia, periostosis, arthralgia, and finger clubbing.
Wegrowski, Yanusz +6 more
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Nepal Journal of Dermatology, Venereology & Leprology, 2016 Pachydermoperiostosis, ( PDP), a rare hereditary disorder that is characterized by digital clubbing, pachydermia, subperiosteal new bone formation, associated with pain, polyarthritis, cutis verticis gyrata, seborrhoea and hyperhidrosis.
S Das, S Chakraborty, NS Sarkar
doaj +3 more sources
Enlarged hands and feet - Not always acromegaly
Indian Journal of Endocrinology and Metabolism, 2012 Pachydermoperiostosis maybe mistaken for acromegaly as it can present with progressive enlargement of hands and feet. We describe a 32 year old male with enlargement of hands and feet and extensive keloid formation.
Vikrant Ghatnatti +2 more
doaj +1 more source
Você conhece esta síndrome? Do you know this syndrome?
Anais Brasileiros de Dermatologia, 2007 Paquidermoperiostose é genodermatose autossômica dominante rara, que afeta pele e ossos, porém sua prevalência e incidência permanecem desconhecidas. Ocorre predominantemente em homens, que também mostram fenótipo mais grave da doença.
Roberta Buense Bedrikow +3 more
doaj +1 more source
Severe complete pachydermoperiostosis (Touraine-Solente-Gole syndrome)
, 2005 BACKGROUND. The thickened, folded skin of Touraine-Solente-Gole syndrome (pachydermoperiostosis) can result in cosmetic and fuctional ...
Aliagaoglu, C, Seyhan, T, Ozerdem, OR
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Familial primary osteoarthropathy: A case report with unusual dental findings
Journal of Indian Academy of Oral Medicine and Radiology, 2015 Pachydermoperiostosis (PDP) is a rare osteo-arthro-dermopathic syndrome, the diagnosis of which can be made on the basis of the classic clinical and radiological presentations.
Vela D Desai +2 more
doaj +1 more source
En coup de sabre accompanied by pachydermoperiostosis: a case report
, 2007 Scleroderma en coup de sabre, a variant of localized scleroderma is a disorder characterized by fibrosis of connective tissue. We report a 21-year-old female with scleroderma en coup de sabre accompanied by pachydermoperiostosis.
Mevlitoglu, I. +2 more
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Pachydermoperiostosis, a unique entity with distinctive clinical features [PDF]
, 2015 Pachydermoperiostosis, which occurs more frequently in men, is a rare entity with distinctive clinical features and an insidious onset.. We report the case of a 30-year-old man with a one-year history of acropachy, arthralgias, hiperhidrosis, and ...
Dominguez-Cherit, Judith +2 more
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A Case of Hypertrophic Gastropathy and Early Gastric Cancer Associated with Pachydermoperiostosis [PDF]
, 2000 Pachydermoperiostosis is a rare hereditary syndrome characterized by finger clubbing, periosteal new bone formation of tubular bones, and hypertrophic skin changes (pachydermia).
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