Results 51 to 60 of about 740 (177)
Anales de la Facultad de MedicinaPachydermoperiostosis, also known as primary hypertrophic osteoarthropathy, is a rare hereditary disease characterized by soft tissue proliferation and periosteal new bone formation in long bones, classically presenting with digital clubbing, symmetric
Victor Sudário Takahashi +3 more
doaj +1 more source
Pachydermoperiostosis-Like Disease In Captive Red Ruffled Lemurs (Varecia Variegatus Rubra) [PDF]
, 2011 Pachydermatoperiostosis, a rare form of hypertrophic osteoarthropathy, is of unknown etiology and previously thought limited to humans. The only periosteal reaction previously reported in prosimians is related to renal disease.
Bruce Rothschild +2 more
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Touraine-Solente-Gole Syndrome: A Rare Case Report
Delhi Journal of Ophthalmology, 2017 Touraine-Solente-Gole Syndrome, also known as Pachydermoperiostosis (PDP) or Primary Hypertrophic Osteoarthropathy, is a rare hereditary disorder, which affects both bones and skin.
Dharmil Doshi +2 more
doaj +1 more source
Trends in Urology &Men's Health, Volume 16, Issue 4, August 2025.ABSTRACT Primary hypertrophic osteoarthropathy (Pachydermoperiostosis) is a rare, inherited genetic disorder of the skeleton and the skin, characterised by clubbing of the fingers, thickening of the skin especially of the face and forehead (pachydermia) and periostosis. Patients often present with pain and swelling of the knees and ankles.
Ahmed AbdulBari +3 more
wiley +1 more source
A rare cause of digital clubbing: pachydermoperiostosis
The Pan African Medical Journal, 2016 A 35-year-old man of Tunisian origin complained of inflammatory arthralgia and he had noticed a progressive enlargement of his hands and feet as well as facial furrowing.
Zeineb Alaya, Walid Osman
doaj +1 more source
A Rare Case: Touraine Solente Gole Syndrome
Haseki Tıp Bülteni, 2017 Touraine-Solente-Gole syndrome, also known as pachydermoperiostosis, is transmitted as an autosomal recessive trait. It is characterized by enlargement of fingers and toes, pachyderma, excessive sweating, and pain.
Kamil Şahin +4 more
doaj +1 more source
Crohn’s disease associated with pachydermoperiostosis [PDF]
, 1999 Pachydermoperiostosis is a rare hereditary syndrome characterized by finger clubbing, periosteal change, pachydermia and autonomic nervous system symptoms such as facial flushing and hy perhidrosis.
김원호
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Pseudoacromegaly—A challenging entity in the endocrine clinic: A systematic review
Clinical Endocrinology, Volume 100, Issue 6, Page 542-557, June 2024.Abstract Objective Pseudoacromegaly encompasses conditions with features of acromegaly/gigantism, but no growth hormone (GH) or insulin‐like growth factor‐1 (IGF‐1) excess. We aimed to review published pseudoacromegaly cases evaluated due to clinical suspicion of acromegaly.
Pedro Marques +2 more
wiley +1 more source
Pachydermoperiostosis ('Touraine-Solente-Gole' Syndrome)
Nepal Journal of Dermatology, Venereology & Leprology, 2013 DOI: http://dx.doi.org/10.3126/njdvl.v11i1.7937 Nepal Journal of Dermatology, Venereology & Leprology Vol.11(1) 2013 pp.64 ...
R Sharma +3 more
doaj +3 more sources
Biologics for inherited disorders of keratinisation: A systematic review
Australasian Journal of Dermatology, Volume 65, Issue 2, Page 185-214, March 2024.Abstract Background/Objectives Recent literature highlights the potential of biologics in the management of inherited disorders of keratinisation. In this study, we conducted a systematic review of existing literature on treatment outcomes of inherited keratinisation disorders treated with biologics.
Michelle K. Y. Chen +3 more
wiley +1 more source