Results 11 to 20 of about 176 (89)
Touraine-Solente-Gole Syndrome: A Rare Case Report
Delhi Journal of Ophthalmology, 2017 Touraine-Solente-Gole Syndrome, also known as Pachydermoperiostosis (PDP) or Primary Hypertrophic Osteoarthropathy, is a rare hereditary disorder, which affects both bones and skin.
Dharmil Doshi +2 more
doaj +5 more sources
A Rare Case: Touraine Solente Gole Syndrome
Haseki Tıp Bülteni, 2017 Touraine-Solente-Gole syndrome, also known as pachydermoperiostosis, is transmitted as an autosomal recessive trait. It is characterized by enlargement of fingers and toes, pachyderma, excessive sweating, and pain.
Kamil Şahin +4 more
doaj +4 more sources
Touraine-Solente-Gole syndrome: The complete form needs to be recognized.
Indian J Nucl Med, 2012 The primary hypertrophic osteoarthropathy (HOA) (pachydermoperiostosis) is a rare hereditary disease characterized by skin manifestations (pachydermia), digital clubbing and proliferation of periosteum (periostitis) with sub-periosteal new bone formation.
Karnan S +3 more
europepmc +5 more sources
Coexistence of Touraine-Solente-Gole syndrome and type 1 neurofibromatosis: A case report
Turkderm Turkish Archives of Dermatology and Venereology, 2021 Pachydermoperiostosis is a rare syndrome that affects the skin and skeletal system. Mutations in the gene encoding hydroxyprostaglandin dehydrogenase (HPGD) are thought to play a role in disease etiopathogenesis.
Selma Korkmaz +5 more
doaj +7 more sources
Frontal lifting using a tissue expander in pachydermoperiostosis: A case report. [PDF]
Clin Case Rep, 2021 Pachydermoperiostosis, a rare condition, is characterized by pachydermia, finger clubbing, and periostosis. We present an unusual treatment for frontal rhytids, for which we used a tissue expander that contributed to thinning of the skin and the depth of the rhytids prior to frontal lifting. The results were maintained after one year.
Cunha DJD +4 more
europepmc +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 +3 more
doaj +4 more sources
Journal of the Dow University of Health SciencesPachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy (PHO), also known as the Touraine–Solente–Gole syndrome, is an autosomal dominant genetic disorder that is rare and is identified by finger clubbing, skin thickening, and periosteal ...
Fatima Khurshid +3 more
doaj +12 more sources
Cutis verticis gyrata as a clinical manifestation of Touraine-Solente-Gole' syndrome (pachydermoperiostosis). [PDF]
BMJ Case Rep, 2013 Cutis verticis gyrata is a descriptive term for a condition of the scalp consisting of deep grooves and convolutions that resemble the surface of the brain. We present a case of a 22-year-old man who presented with pain and swelling of both knees and hands.
Sandoval AR +5 more
europepmc +4 more sources
Comprehensive Treatment of a Rare Case of Complete Primary Pachydermoperiostosis with Large Facial Keloid Scars: A Case Report and Literature Review [PDF]
Case Reports in DermatologyIntroduction: Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy, is a rare autosomal dominant disease with primary clinical features of pachydermia (thickening of skin) and periostosis (new bone formation).
Haibo Zhao +3 more
doaj +2 more sources
Primary Idiopathic Osteoarthropathy: Could It Be Related to Alcoholism? [PDF]
Case Rep Rheumatol, 2017 Background. Hypertrophic osteoarthropathy (HOA) is a syndrome characterized by abnormal proliferation of the skin and bony structures at the distal extremities resulting in digital clubbing, periosteal bony reaction, and joint effusion. It can be primary (idiopathic) without any clear identifiable etiology as well as secondary to variety of systemic ...
Alnimer Y +3 more
europepmc +2 more sources