Results 51 to 60 of about 547 (180)
Pachydermoperiostosis-Like Disease In Captive Red Ruffled Lemurs (Varecia Variegatus Rubra) [PDF]
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
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
Biological Stress and Age-at-Death: Differential Survivorship in Colonial Period North Coast Peru
The relationship between age at death and biological stress experience is vital to consider, especially in the bioarchaeology of Colonial Latin America, where drastic changes in indigenous health and population size followed European contact. This thesis
Phillips, Megann
core +1 more source
Primary Hypertrophic Osteoarthropathy: A Case Series
Primary hypertrophic osteoarthropathy (PHOA) is a rare genetic disorder defined by digital clubbing, periostosis of long bones, and musculoskeletal pain.
Ramakant Singh +6 more
doaj +1 more source
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
Form fruste pachydermoperiostosis associated with ptosis and floppy eyelid syndrome
Pachydermoperiostosis (PDP), also known as idiopathic or primary hypertrophic osteoarthropathy or Touraine-Solente-Gole Syndrome, is a rare genetic disorder affecting skin and bone, consisting of pachydermia and periostosis.
Rubinov, Avi +4 more
core +1 more source
Bone Research Society 2021 Abstracts
JBMR Plus, Volume 5, Issue S5, November 2021.
wiley +1 more source
Introduction Pachydermoperiostosis or primary hypertrophic osteoathropathy is a rare genetic disease with autosomal transmission. This disorder, which affects both bones and skin, is characterized by the association of dermatologic changes (pachydermia ...
Akrout Rim +5 more
doaj +1 more source

