Primary hypertrophic osteoarthropathy and bilateral transient lateral patellar dislocation in an adolescent. [PDF]
This case report is of the index case of bilateral transient patellar dislocation in a patient with primary hypertrophic osteoarthropathy. Primary hypertrophic osteoarthropathy is a rare complex disorder with variable presentation and thus frequently ...
Jeyabaladevan S+3 more
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Clubbing of Fingers and Nails in Primary Hypertrophic Osteoarthropathy Type 1. [PDF]
Pauly M+2 more
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Primary lymphosarcoma of lung associated with hypertrophic pulmonary osteoarthropathy. [PDF]
G. F. A. Benfield
openaire +5 more sources
Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy. [PDF]
Zhang Z+13 more
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Hypertrophic osteoarthropathy (HOA) is a condition characterized by aberrant skin and osseous tissue proliferation in the distal extremities. Mutations in the 15-hydroxyprostaglandin dehydrogenase gene (HPGD) and the soluble carrier organic anion carrier
Ilke Coskun Benlidayi+2 more
doaj +1 more source
SLCO2A1 gene is the causal gene for both primary hypertrophic osteoarthropathy and hereditary chronic enteropathy. [PDF]
Umeno J+4 more
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Hypertrophy of the feet and ankles presenting in primary hypertrophic osteoarthropathy or pachydermoperiostosis: a case report. [PDF]
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 R+5 more
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Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy. [PDF]
Guo T+5 more
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Characterization of Mineral and Bone Metabolism Biomarkers in a Chinese Consanguineous Twin Family with Primary Hypertrophic Osteoarthropathy. [PDF]
Purpose Primary hypertrophic osteoarthropathy (PHO) is a rare, autosomal, recessive genetic disease characterized by digital clubbing, periostosis, and pachydermia. The underlying cause for the pathogenesis of this disease is a defect in prostaglandin E2
Li N+7 more
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