Results 1 to 10 of about 184 (89)
Touraine–Solente–Gole syndrome: Clinical manifestation with bilateral true eyelid ptosis [PDF]
JPRAS Open, 2019 Touraine–Solente–Gole syndrome (pachydermoperiostosis [PDP] or primary idiopathic hypertrophic osteoarthropathy [HOA]) is a rare hereditary disorder that is characterized by a triad of manifestations that consists of skin changes (pachydermia), abnormal ...
Nutthawut Akaranuchat +1 more
doaj +6 more sources
Touraine Solente Gole syndrome: The elephant skin disease
Indian Journal of Plastic Surgery, 2013 Touraine Solente Gole syndrome is a rare hereditary syndrome of primary pachydermoperiostosis, with the characteristic triad of pachydermia (or elephant like skin), periostosis and acropachia.
T. M. Sheeja Rajan +3 more
doaj +6 more sources
Touraine–Solente–Gole’ syndrome [PDF]
Case Reports, 2011 Touraine–Solente–Gole’ syndrome, also known as pachydermoperiostosis or primary hypertrophic osteoarthropathy is a rare familial disorder generally seen in males. Although it presents with characteristic morphological and radiological features, this is an uncommon diagnosis and is entertained only once other causes of secondary hypertrophic ...
Monica Gupta, S S Lehl
exaly +6 more sources
Pachydermoperiostosis (Touraine–Solente–Gole syndrome): a case report [PDF]
Journal of Medical Case Reports, 2019 Background Pachydermoperiostosis (PDP) is a rare disorder characterized by clubbing of the fingers, thickening of the skin (pachyderma), and excessive sweating (hyperhidrosis).
Amir Joshi +4 more
doaj +5 more sources
Familial Touraine-Solente-Gole syndrome [PDF]
BMJ Case Reports, 2022 Touraine-Solente-Gole syndrome is a rare, autosomal dominant multisystem disorder arising from dysregulated prostaglandin synthesis due to underlying genetic defects. Early symptoms are related to skin and soft tissue involvement (coarse facial features, widening of wrists, etc) and may thus be overlooked unless a careful physical examination is ...
Mahendra singh Rajput +2 more
exaly +4 more sources
Touraine-Solente-Gole syndrome: pathogenic variant in SLCO2A1 presented with polyarthralgia and digital clubbing [PDF]
Pediatric Rheumatology Online Journal, 2023 Background Primary Hypertrophic Osteoarthropathy (PHO), also known as Touraine-Solente-Gole Syndrome, is a rare, multisystemic autosomal recessive disorder caused by pathogenic variants in the 15-hydroxyprostaglandin dehydrogenase (HPGD) or Solute ...
Rafaela Nicolau +7 more
doaj +4 more sources
Touraine-Solente-Gole syndrome [PDF]
BMJ Case Reports, 2019 A 26-year-old man presented to our clinic with gradually progressive painful swelling of wrists, knees and ankles for the last 10 years. Since the last 2 years, he had also noticed an increase in thickness of skin over his forehead and an increase in sweating over his palms and feet.
Nitin Gupta, Ankit Mittal, Manish Soneja
exaly +5 more sources
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
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