Results 41 to 50 of about 752 (202)
Reumatismo, 2014 Pachydermoperiostosis is a rare hereditary disorder, which affects both bones and skin. It is characterized by a combination of dermatologic changes (pachydermia or thickening of the skin) and rheumatologic manifestations (periostosis and finger clubbing)
S. El Aoud +4 more
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A rare case of pachydermoperiostosis associated with blepharoptosis and floppy eyelids
Indian Journal of Ophthalmology, 2016 Pachydermoperiostosis (PDP) is a multisystem disorder of mesenchymal origin. It is a form of hypertrophic osteoarthropathy. The typical clinical features include pachydermia, cutis verticus gyrata, digital clubbing, and periostosis. Patients present with
Bipasha Mukherjee, Md. Shahid Alam
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Collective secondary cremation in a pit grave: a unique funerary context in Portuguese Chalcolithic burial practices [PDF]
, 2014 Perdigões is a large site with a set of ditched enclosures located at Reguengos de Monsaraz, Alentejo, South Portugal. Recently at the central area of this site burnt human remains were found in a pit (#16).
Costa, C. +4 more
core +1 more source
Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey
JCRPE, 2022 Pachydermoperiostosis (PDP), also known as primary hypertrophic osteoarthropathy, is a rare genetic disorder characterized by pachyderma and periostosis.
Emine Kartal Baykan, Ayberk Türkyılmaz
doaj +1 more source
Journal of the Dow University of Health SciencesPachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy (PHO), also known as the Touraine–Solente–Gole syndrome, is an autosomal dominant genetic disorder that is rare and is identified by finger clubbing, skin thickening, and periosteal ...
Fatima Khurshid +3 more
doaj +9 more sources
Endocrine Connections, 2019 Background: Primary hypertrophic osteoarthropathy (PHO) is a rare genetic multi-organic disease characterized by digital clubbing, periostosis and pachydermia. Two genes, HPGD and SLCO2A1, which encodes 15-hydroxyprostaglandin dehydrogenase (15-PGDH) and
Qianqian Pang +8 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
core +1 more source
American Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.ABSTRACT Primary Hypertrophic Osteoarthropathy (PHOAR1) is characterized by autosomal recessive loss of function variants in 15‐hydroxyprostaglandin dehydrogenase (HPGD) leading to digital clubbing, periostosis, pachydermia, and severe hyperhidrosis. HPGD catalyzes the first step of prostaglandin E2 (PGE2) degradation.
Kara Zehr +6 more
wiley +1 more source
Gastric Juvenile Polyposis with High-Grade Dysplasia in Pachydermoperiostosis
Case Reports in Gastroenterology, 2011 Pachydermoperiostosis (PDP) is the primary form of hypertrophic osteoarthropathy. It is a very rare disease consisting of pachydermia, digital clubbing and radiologic periostosis.
L. de Mestier +5 more
doaj +1 more source