Results 41 to 50 of about 8,832 (185)

Primary hypertrophic osteoarthropathy and bilateral transient lateral patellar dislocation in an adolescent. [PDF]

open access: yesBJR Case Rep, 2022
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
europepmc   +2 more sources

Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy. [PDF]

open access: bronzeAm J Hum Genet, 2012
Zhang Z   +13 more
europepmc   +2 more sources

HYPERTROPHIC OSTEOARTHROPATHY IN A PATIENT WITH HETEROZYGOUS MUTATION IN THE SLCO2A1 GENE: A CASE REPORT

open access: yesCentral Asian Journal of Medical Hypotheses and Ethics, 2023
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

Hypertrophy of the feet and ankles presenting in primary hypertrophic osteoarthropathy or pachydermoperiostosis: a case report. [PDF]

open access: yesJ Med Case Rep, 2012
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
europepmc   +2 more sources

Characterization of Mineral and Bone Metabolism Biomarkers in a Chinese Consanguineous Twin Family with Primary Hypertrophic Osteoarthropathy. [PDF]

open access: yesInt J Endocrinol, 2020
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
europepmc   +2 more sources

Home - About - Disclaimer - Privacy