Results 41 to 50 of about 808 (216)
A community in transition: Analysis of health and well‐being in people living during and following aridification [PDF]
This paper considers skeletal and dental lesions to assess the effects of aridification on two skeletal samples from the Bronze Age in what is now the United Arab Emirates (UAE), located on the eastern end of the Arabian Peninsula.
Caine, Alyson C. +2 more
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A rare cause of digital clubbing: pachydermoperiostosis
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
Mortuary Practices and Social Identity at Matrix 101, La Leche Valley, Peru [PDF]
This thesis focuses on the social identity of the individuals buried at a Late Middle Sicán (A.D. 1050-1120) mass grave designated Matrix 101. Matrix 101 is located in the Great Plaza of the Pomac forest archaeological complex in the La Leche Valley ...
Hurtubise, Jenna Renee
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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
doaj +1 more source
A rare case of pachydermoperiostosis associated with blepharoptosis and floppy eyelids
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
doaj +1 more source
Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey
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
Pachydermoperiostosis (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
The necropolis at the Cathedral Hill in Vyazma is mainly dated to the late 13th c. AD, and likely contains burials of the citizens of a high social status.
Andrey A. Evteev, Anna A. Tarasova
doaj +1 more source
A case of finger clubbing associated with nasopharyngeal carcinoma in a young girl, and review of pathophysiology [PDF]
Hypertrophic osteoarthropathy is characterized by clubbing of the digital tips and periosteal reaction of long bones. Most of the cases are associated with malignancy or other conditions such as congenital heart disease, liver cirrhosis, pulmonary ...
Abbasi, Ahmed Nadeem +5 more
core +1 more source

