Results 31 to 40 of about 6,845 (196)
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
Primary hypertrophic osteoarthropathy
The article presents information about a rare hereditary disease – primary hypertrophic osteoarthropathy with autosomal dominant and autosomal recessive inheritance.
E. L. Trisvetova
doaj +1 more source
Collagen‐Based Hydrogels for Cartilage Regeneration
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
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
Schizophrenia is associated to somatic disorders especially cardio‐vascular and auto‐immune. Through this case report, we describe an association with hypertrophic osteoarthropathy (HPO).
Emna Baklouti +3 more
doaj +1 more source
Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report
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
Nosology of genetic skeletal disorders: 2023 revision
Abstract The “Nosology of genetic skeletal disorders” has undergone its 11th revision and now contains 771 entries associated with 552 genes reflecting advances in molecular delineation of new disorders thanks to advances in DNA sequencing technology.
Sheila Unger +20 more
wiley +1 more source
A case report of an extremely rare association of ankylosing spondylitis with pachydermoperiostosis
Key Clinical Message We describe a case of a young man with features of pachydermoperiostosis and spondyloarthropathy. By describing this rarity, we aim to help build a database for future studies and construct a management plan that rheumatologists and clinicians can use.
Faiq I. Gorial +2 more
wiley +1 more source
Osteoartropatia hipertrófica secundária a neoplasia pulmonar: Relato de caso
Resumo: A osteoartropatia hipertrófica secundária é uma alteração sistémica que acomete os ossos, as articulações e as partes moles, sendo secundária a alguma patologia intratorácica.
Angelo Ferreira da Silva Junior +5 more
doaj +1 more source
The SIRT3‐medicated post‐translational acetylation of the mitochondrial respiratory chain has therapeutic potential for the treatment of osteoarthritis (OA). Mechanistically, SIRT3 directly binds and deacetylates COX4I2 to promote mitochondrial respiration activity.
Yijian Zhang +12 more
wiley +1 more source

