Results 21 to 30 of about 176 (89)

Distinct features of three clinical subtypes in 533 patients with primary hypertrophic osteoarthropathy [PDF]

Orphanet Journal of Rare Diseases
Background Primary hypertrophic osteoarthropathy (PHO) is a rare genetic disorder classified into clinical subtypes and genetic subtypes. Previous clinical studies have primarily focused on case reports and family analyses, largely characterizing the ...
Xilei Cai, Xiujuan Yang, Pengyue Zhang, Ziyue Dou, Zilian Chen, Chongzhi Zhu, Weiwei Xu, Xinchen Wang, Xiaodan Hong, Zhenhua Zhang   +9 more
doaj   +2 more sources

Tc-99m MDP bone scintigraphy in a case of Touraine-Solente-Gole syndrome.

Indian J Nucl Med, 2011
Pachydermoperiostosis is a form of primary hypertrophic osteoarthropathy, also known as Touraine-Solente-Gole syndrome. It is a rare disease. In this report, we present the case of a 29-year-old man with this rare disorder, having significant findings on Tc-99m methylene diphosphonate bone scan.
Mudalsha R, Jacob M, Jora C, Pandit A.
europepmc   +3 more sources

Pachydermoperiostosis mimicking acromegaly: A case report

Indian Dermatology Online Journal, 2018
Pachydermoperiostosis is a rare, hereditary disease commonly presenting with digital clubbing, pachyderma, and periosteal hypertrophy. Coarsening of facial features and spade-like enlargement of hands and feet may give rise to a diagnostic dilemma ...
Prerna, Romana Ghosh, Jayanta K Barua, Arup K Das   +3 more
doaj   +2 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
The primary hypertrophic osteoarthropathy (PHOA) (pachydermoperiostosis) is a rare genetic/hereditary disease characterized by skin changes (pachydermia), clubbing of fingers and periosteal thickening (periostitis) with sub-periosteal new bone formation. Here we describe a case of an adolescent male who presented with clubbing and polyarthralgia.
Sivathapandi T, Amalachandran J, Simon S, Elangovan I.   +3 more
europepmc   +4 more sources

Touraine-Solente-Gole syndrome with acne vulgaris successfully treated with isotretinoin [PDF]

Journal of Dermatology & Cosmetology, 2018
Touraine Solente Gole syndrome or pachydermoperiostosis is a rare genodermatosis affecting skin bones and connective tissue characterized by the triad of pachydermia periostosis and digital clubbing The authors report the case of a year old man presenting the dermato rheumatic symptoms that characterize the complete form of the syndrome He also ...
openaire   +3 more sources

Touraine-Solente-Gole syndrome.

Saudi medical journal, 2004
exaly   +5 more sources

Touraine-Solente-Gole Syndrome- A Rare Cause of Familial Periostosis

Journal of Evolution of Medical and Dental Sciences, 2020
Ajay Sharawat, Girendra Shankar, Kamal Kumar Sen, Tamanna Tamanna   +3 more
openaire   +3 more sources

Complete form of pachydermoperiostosis in a 16-year-old boy: A case report

Indian Journal of Paediatric Dermatology, 2022
Pachydermoperiostosis is an inherited osseocutaneous disorder. The unusual increased levels of prostaglandin E2 due to mutations in either HPGD gene or SLCO2A1 gene are regarded as the causative factor.
Sahana M Srinivas, Suman Swamynathan, Vani Hebbal Nagarajappa, Raghupathy Palany   +3 more
doaj   +1 more source

Complete pachydermoperiostosis with diffuse keratoderma mimicking thyroid Acropachy: A case report and review of literature

Ibom Medical Journal, 2023
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, Owolabi FA, Ologun O, Oninla OA, Enitan A, Olasode O   +5 more
doaj   +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