Results 21 to 30 of about 1,313 (164)

Primary hypertrophic osteoarthropathy

Научно-практическая ревматология, 2020
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

Case report: Schizophrenia and hypertrophic osteoarthropathy, a rare syndrome hiding a life‐threatening condition

Clinical Case Reports, 2022
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, Mehdi Karoui, Rania Kammoun, Faten Ellouze   +3 more
doaj   +1 more source

Collagen‐Based Hydrogels for Cartilage Regeneration

Orthopaedic 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, Yan Xu, Yu Han, Jing Cui, Zheng Jing, Dongbo Li, Jianguo Liu, Chunsheng Xiao, Dongsong Li, Bo Cai   +9 more
wiley   +1 more source

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

JBMR 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

Pierre Marie–Bamberger syndrome (secondary hypertrophic osteoarthropathy) [PDF]

International Journal of Dermatology, 2004
A 55‐year‐old man presented to our Department with a 10‐year history of coarsening of the facial features. The soft tissue of the forehead had become progressively thickened and corrugated, resulting in marked, hard‐elastic asymmetrical convolutions involving the underlying eyelids, with partial reduction of the visual field (Fig. 1a,b).
CANNAVO', Serafinella, GUARNERI, Claudio, BORGIA, Francesco, VACCARO, Mario   +3 more
openaire   +3 more sources

Osteoartropatia hipertrófica secundária a neoplasia pulmonar: Relato de caso

Revista Portuguesa de Pneumologia, 2009
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, Eduardo Garcia, Fabíola Schorr, Amanda Barreto da Silva, Lucas Medeiros, Andre Barreto da Silva   +5 more
doaj   +1 more source

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

Clinical 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, Ayam Bhattarai, Bibek Devkota, Saurav Khatiwada, Pramod Kumar Kafle, Achyut Krishna Phuyal, Manoj Shahi   +6 more
wiley   +1 more source

Pharmacology update: pamidronate for hypertrophic pulmonary osteoarthropathy in palliative care

Therapeutic Advances in Rare Disease, 2022
Hypertrophic pulmonary osteoarthropathy (HPOA) is a rare syndrome that causes clubbed fingers, periostitis, and synovial effusions. It can adversely impact a patient’s quality of life.
Bethany Faust, Aaron Parkinson, Steven J. Baumrucker   +2 more
doaj   +1 more source

Nosology of genetic skeletal disorders: 2023 revision

American Journal of Medical Genetics Part A, Volume 191, Issue 5, Page 1164-1209, May 2023., 2023
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, Carlos R. Ferreira, Geert R. Mortier, Houda Ali, Débora R. Bertola, Alistair Calder, Daniel H. Cohn, Valerie Cormier‐Daire, Katta M. Girisha, Christine Hall, Deborah Krakow, Outi Makitie, Stefan Mundlos, Gen Nishimura, Stephen P. Robertson, Ravi Savarirayan, David Sillence, Marleen Simon, V. Reid Sutton, Matthew L. Warman, Andrea Superti‐Furga   +20 more
wiley   +1 more source

A case report of an extremely rare association of ankylosing spondylitis with pachydermoperiostosis

Clinical Case Reports, Volume 11, Issue 5, May 2023., 2023
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, Nabaa Ihsan Awadh, Maryam A. Hamzah   +2 more
wiley   +1 more source