Results 51 to 60 of about 10,313 (226)

Gastric Juvenile Polyposis with High-Grade Dysplasia in Pachydermoperiostosis [PDF]

Case Reports in Gastroenterology, 2011
Pachydermoperiostosis (PDP) is the primary form of hypertrophic osteoarthropathy. It is a very rare disease consisting of pachydermia, digital clubbing and radiologic periostosis.
L. de Mestier, S. Moreau, C. Neuzillet, P. Ruszniewski, Y. Panis, P. Hammel   +5 more
doaj   +4 more sources

Novel Pathogenic Variants in SLCO2A1 Causing Autosomal Dominant Primary Hypertrophic Osteoarthropathy

European Journal of Medical Genetics, 2022
Primary hypertrophic osteoarthropathy (PHO), or pachydermoperiostosis, is characterized by a clinical association including digital clubbing, periostosis and pachydermia. SLCO2A1 and HPGD genes are both responsible for PHO.
Adrien Bloch, Guillaume Couture, Bertrand Isidor, Manon Ricquebourg, E. Bourrat, Dan Lipsker, B Taillan, Alice Combier, C. Chiavérini, Bruno Delobel, Pascal Richette, Corinne Collet   +11 more
openalex   +2 more sources

Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy. [PDF]

Mol Med Rep, 2017
Guo T, Yang K, Liu L, Tan ZP, Luo H, Luo H.   +5 more
europepmc   +3 more sources

The Clinical Spectrum of Pachydermoperiostosis (Primary Hypertrophic Osteoarthropathy)

Medicine, 1991
The clinical spectrum of pachydermoperiostosis (primary hypertrophic osteoarthropathy).
Marco Matucci‐Cerinic, Torello Lotti, Ivo Jajić, Alberto Moggi Pignone, Cecilia Bussani, M Cagnoni   +5 more
openalex   +5 more sources

Primary Hypertrophic Osteoarthropathy: A Case Report

Case Reports in Clinical Practice, 2018
The primary hypertrophic osteoarthropathy (PHOA or pachydermoperiostosis) is a rare (5% of total HOA) hereditary disease. One study described that the prevalence of PHOA is 0.16%.
Shima Asadi-Komeleh, Abdolrahman Rostamian, Fatemeh Shahbazi, Shafieh Movassagi, Parviz Soofivand   +4 more
doaj   +1 more source

A Loss-of-Function Variant Causing Primary Autosomal Recessive Hypertrophic Osteoarthropathy. [PDF]

Cureus
Patel DN, Sidlow R.
europepmc   +3 more sources

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

Am J Hum Genet, 2012
Zhang Z, Xia W, He J, Zhang Z, Ke Y, Yue H, Wang C, Zhang H, Gu J, Hu W, Fu W, Hu Y, Li M, Liu Y.   +13 more
europepmc   +3 more sources

Myelofibrosis as a Presenting Manifestation of Primary Hypertrophic Osteoarthropathy

Indian Journal of Hematology and Blood Transfusion
Paras Gupta, Sarthak Wadhera, Anish Bhattacharya, Namrata Kaul, Arihant Jain, Jasmina Ahluwalia, Pankaj Malhotra   +6 more
openalex   +3 more sources

Incomplete form of Primary Hypertrophic Osteoarthropathy (Touraine-Solente-Gole Syndrome) Masquerading as Polyartrhalgia Diagnosed in Technetium-99m-Methylene Diphosphonate Scintigraphy: An Interesting Case Report.

Indian J Nucl Med, 2018
Sivathapandi T, Amalachandran J, Simon S, Elangovan I.   +3 more
europepmc   +3 more sources

Osteological and Biomolecular Evidence of a 7000-Year-Old Case of Hypertrophic Pulmonary Osteopathy Secondary to Tuberculosis from Neolithic Hungary [PDF]

, 2013
Seventy-one individuals from the late Neolithic population of the 7000-year-old site of Hódmezővásárhely-Gorzsa were examined for their skeletal palaeopathology.
Besra, GS, Bull, ID, Donoghue, HD, Lee, OY-C, Masson, M, Minnikin, DE, Molnar, E, Palfi, G, Wu, HHT   +8 more
core   +7 more sources