Results 31 to 40 of about 87,294 (214)

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

Hypertrophic osteoarthropathy

open access: hybridMedicina Clínica (English Edition), 2018
Sonia, Osorio Aira   +3 more
openaire   +3 more sources

Palindromic rheumatism associated with primary hypertrophic osteoarthropathy

open access: greenClinics, 2006
Samuel Katsuyuki Shinjo   +2 more
doaj   +3 more sources

Monoallelic mutations in SLCO2A1 cause autosomal dominant primary hypertrophic osteoarthropathy

open access: yesJournal of Bone and Mineral Research, 2021
Primary hypertrophic osteoarthropathy (PHO) is a rare disease inherited as a recessive or irregular dominant trait and characterized by digital clubbing, pachydermia, and periostosis.
Yang Xu   +4 more
semanticscholar   +1 more source

Collagen‐Based Hydrogels for Cartilage Regeneration

open access: yesOrthopaedic Surgery, Volume 15, Issue 12, Page 3026-3045, December 2023., 2023
This review provided an overview of the progress made in research on collagen hydrogels with chondrocytes or stem cells, comprehensively covered the research progress and clinical applications of collagen‐based hydrogels that integrated inorganic or organic materials. Cartilage regeneration remains difficult due to a lack of blood vessels.
Lihui Sun   +9 more
wiley   +1 more source

Complete pachydermoperiostosis with diffuse keratoderma mimicking thyroid Acropachy: A case report and review of literature

open access: yesIbom Medical Journal, 2023
Pachydermoperiostosis (PDP) is a rare genodermatosis with prominent cutaneous, soft tissue and skeletal manifestations. It can mimic secondary causes of hypertrophic osteoarthropathy such as thyroid acropachy.
Ajani AA   +5 more
doaj   +1 more source

Biomechanical Impact of Phosphate Wasting on Articular Cartilage Using the Murine Hyp Model of X‐linked hypophosphatemia

open access: yesJBMR Plus, Volume 7, Issue 10, October 2023., 2023
ABSTRACT Degenerative osteoarthritis (OA) is recognized as an early‐onset comorbidity of X‐linked hypophosphatemia (XLH), contributing to pain and stiffness and limiting range of motion and activities of daily living. Here, we extend prior findings describing biochemical and cellular changes of articular cartilage (AC) in the phosphate‐wasting ...
Carolyn M Macica, Steven M Tommasini
wiley   +1 more source

Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report

open access: yesClinical Case Reports, Volume 11, Issue 6, June 2023., 2023
X‐ray of hand showing cortical thickening and periosteal reaction in distal radius ulna and phalynges of hand of a patient with pachydermoperiostosis. Key Clinical Message Pachydermoperiostosis is a rare genetic disorder that closely resembles acromegaly. Diagnosis is usually based on distinct clinical and radiological features. Oral etoricoxib therapy
Abinash Baniya   +6 more
wiley   +1 more source

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