Results 21 to 30 of about 2,266 (189)

Clinical and genetic characteristics of primary hypertrophic osteoarthropathy

Нервно-мышечные болезни, 2023
Background. Primary hypertrophic osteoarthropathy is a rare genetically heterogeneous disease with three clinical variants. The classic one is a combination of hyperostosis, arthropathy and pachyderma and two variants with damage to only bone structures ...
E. L. Dadali, T. V. Markova, V. M. Kenis, T. S. Nagornova, S. S. Nikitin   +4 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

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

Pachydermoperiostosis in a patient with chronic hepatitis B virus infection referred as acromegaly: a case report

Journal of Medical Case Reports, 2018
Background Primary hypertrophic osteoarthropathy also known as pachydermoperiostosis is a rare genetic disorder that has often been confused with acromegaly because of similar clinical features.
Yacoba Atiase, Ernest Yorke, Josephine Akpalu, Bismark Opoku-Asare, Patrick Adjei, Maame Boatemma Amissah-Arthur, Albert Akpalu   +6 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

Familial primary osteoarthropathy: A case report with unusual dental findings

Journal of Indian Academy of Oral Medicine and Radiology, 2015
Pachydermoperiostosis (PDP) is a rare osteo-arthro-dermopathic syndrome, the diagnosis of which can be made on the basis of the classic clinical and radiological presentations.
Vela D Desai, Sunil MV Kumar, Sahil Maghu   +2 more
doaj   +1 more source

Hypertrophic osteopathy in a cat with a concurrent injection-site sarcoma. [PDF]

, 2015
Case summary An 11-year old neutered female domestic shorthair cat presented for investigation of a large, partially ulcerated skin mass in the area of the left scapula. The cat had been vaccinated 6 weeks previously in the same area.
Constantino-Casas, Fernando, Demetriou, Jackie, Herrtage, Michael, Salgüero, Raquel   +3 more
core   +2 more sources

Pachydermoperiostosis ('Touraine-Solente-Gole' Syndrome)

Nepal Journal of Dermatology, Venereology & Leprology, 2013
DOI: http://dx.doi.org/10.3126/njdvl.v11i1.7937 Nepal Journal of Dermatology, Venereology & Leprology Vol.11(1) 2013 pp.64 ...
R Sharma, S Pandey, D Choudhary, DB Pokhrel   +3 more
doaj   +3 more sources

Primary Hypertrophic Osteoarthropathy With Myelofibrosis

Cureus, 2022
Primary hypertrophic osteoarthropathy (PHO) is a rare autosomal recessive inherited multi-system disorder characterized by a triad of pachydermia, periostosis, and clubbing. PHO was revealed to be caused by the HPGD gene producing 15-prostaglandin dehydrogenase and the SLCO2A1 gene expressing one kind of prostaglandin transporter.
Yousaf, Muhammad, Khan, Rubina, Akram, Zaineb, Chaudhry, Qammar U, Iftikhar, Raheel   +4 more
openaire   +2 more sources