Results 31 to 40 of about 176 (89)

Pachydermoperiostosis: a case report

Остеопороз и остеопатии, 2017
Pachydermoperiostosis (PHO) or primary hypertrophic osteoarthropathy is a rare genetic disease that typically begins during childhood or adolescence. It is characterized by digital clubbing, pachydermia and periosteal reaction and progresses gradually ...
Valentina A. Fursenko, Tatiana A. Grebennikova, Alexey G. Nikitin, Zhanna E. Belaya   +3 more
doaj   +1 more source

Ayurveda management of Touraine–Solente–Gole syndrome: A clinical experience

Journal of Ayurveda Case Reports
Touraine–Solente–Gole syndrome, also known as pachydermoperiostosis (PDP) or primary osteoarthropathy, is a rare genetic disorder characterized by a distinctive triad: pachydermia (skin thickening), digital clubbing, and periostosis (excessive bone ...
T. Shrilatha Kamath, Anchumol Joseph
doaj   +1 more source

Primary hypertrophic osteoarthropathy (Touraine-Solente-Gole Syndrome) in newborn: A rare orthopedic condition seen in newborn

Journal of Clinical Neonatology, 2016
Primary hypertrophic osteoarthropathy (PHO), known with various name, is a very rare syndrome, seen infrequently in clinical practice and presents with a wide spectrum of diverse radiological and clinical features in the patient. PHO was first described by Friedreich in 1868 with typical words of “excessive growth of bone of the entire skeleton.” The ...
Deepak Sharma, SunilRaj Pawar, Siluvery Bharathi, Sweta Shastri   +3 more
openaire   +1 more source

Touraine-Solente-Gole syndrome in two siblings.

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2016
Hypertrophic Osteoarthropathy secondary to various causes is not a common entity but primary hypertrophic osteoarthropathy (also called Touraine-Solente-Gole Syndrome) is an extremely rare genetic disorder. It was first described in 1868 by Friedrich and has premier features of clubbing, periostosis and pachydermia.
Aisha, Iftikhar, Muhammad Haroon, Hamid, Ahsan Waheed, Rathore   +2 more
openaire   +1 more source

Complete pachydermoperiostosis (Touraine–Solente–Gole Syndrome) in a young Yemeni man

Journal of Dermatology & Cosmetology
Pachydermoperiostosis (PDP) is a rare genodermatosis, caused by pathogenic variants in the 15-hydroxyprostaglandin dehydrogenase (HPGD) or Solute Carrier Organic Anion Transporter Family Member 2A1 (SLCO2A1) genes, affecting the skin and bones. It is frequently misdiagnosed as acromegaly due to its presentation, which includes digital clubbing, bone ...
Mohammad Ali Alshamia, Ahlam Mohammad Alshami, Hadeel Mohammad Alshami   +2 more
openaire   +1 more source

Pachydermoperiostosis with bilateral ptosis and its associated systemic comorbidities: a rare case report. [PDF]

Pan Afr Med J, 2023
Hlaing SS, Field AY, Mowatt LL, Yee HL, Noguera CM, Palmer GL, Mattis AC, Nelson CC, Fleming JC.   +8 more
europepmc   +1 more source

Pachydermodactyly: Soft Tissue Enlargement of the Fingers in a Teenager. [PDF]

Cureus, 2023
Gallardo-Villamil A, Cano-Aguilar LE, Pérez-Muñoz E, Rojas-Maruri M, Saez de Ocariz M.   +4 more
europepmc   +1 more source

Pachydermoperiostosis and Work Restrictions: A Case Report. [PDF]

Cureus, 2023
Chinichian M, Asghari O, Safaie N, Kassiri N.   +3 more
europepmc   +1 more source

Pachydermoperiostosis: a case report of initial improvement with etoricoxib. [PDF]

Ann Med Surg (Lond), 2023
Vaidya N, Acharya N, Katila S, Adhikari S, Pandey U.   +4 more
europepmc   +1 more source

Primary Hypertrophic Osteoarthropathy With Myelofibrosis. [PDF]

Cureus, 2022
Yousaf M, Khan R, Akram Z, Chaudhry QU, Iftikhar R.   +4 more
europepmc   +1 more source