Results 31 to 40 of about 342 (104)

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.
Sahil Maghu, SunilMV Kumar, VelaD Desai
core   +3 more sources

Touraine-Solente-Gole syndrome: The elephant skin disease.

The National Medical Journal of India, 2023
Sahil Agrawal, Neelima Balakrishnan, S. Modaboyina, Rajeswari Thangavel, D. Das, Saloni Gupta   +5 more
semanticscholar   +3 more sources

Pachydermoperiostosis (Touraine–Solente–Gole syndrome) imitating Acromegaly: A Rare Case Report

Journal of Clinical and Medical Images, Case Reports, 2022
Pachydermoperiostosis (PDP), also known as Touraine-Solente-Golé syndrome/Rosenfeld-Kloepfer syndrome/primary or idiopathic Hypertrophic osteoarthropathy, is an autosomal-dominant/autosomal recessive inherited disorder with variable expression. In its complete form, it is characterized by pachyderma (thickening of the facial skin), skeletal changes ...
null null, Richmond Ronald Gomes
openaire   +2 more sources

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.
Mohammad Ali Alshamia, A. M. Alshami, H. Alshami   +2 more
semanticscholar   +2 more sources

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 ...
D. Sharma, S. Pawar, S. Bharathi, Sweta Shastri   +3 more
semanticscholar   +2 more sources

Touraine-Solente-Gole syndrome.

Saudi medical journal, 2004
core   +4 more sources

Клинико-генетические характеристики первичной гипертрофической остеоартропатии [PDF]

, 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, S. S. Nikitin, T. S. Nagornova, T. V. Markova, V. M. Kenis, В. М. Кенис, Е. Л. Дадали, С. С. Никитин, Т. В. Маркова, Т. С. Нагорнова   +9 more
core   +4 more sources

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

Orphanet J Rare Dis
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 ...
Cai X, Yang X, Zhang P, Dou Z, Chen Z, Zhu C, Xu W, Wang X, Hong X, Zhang Z.   +9 more
europepmc   +2 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

Cutis verticis gyrata in a patient with multiple basal cell carcinomas; case presentation and review of the literature [PDF]

, 2016
Cutis verticis gyrata is a rare disease characterized by convoluted folds and deep furrows of the scalp, resembling the gyri and sulci of the cerebral cortex.
Benea, Vasile, Georgescu, Simona Roxana, Mitran, Cristina Iulia, Mitran, Mădălina Irina, Rusu, Alice, Sârbu, Maria Isabela, Tampa, Mircea   +6 more
core   +4 more sources