Results 21 to 30 of about 568 (137)
ODP341 Pachydermia lesions identified on imaging in a cohort of acromegaly patients [PDF]
Journal of the Endocrine Society, 2022 exaly +1 more source
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 +3 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 +1 more source
Современная ревматология, 2018 The paper gives the data available in the literature on the relatively rare disease hypertrophic osteoarthropathy (HOA). This syndrome includes symptoms, such as clubbed fingers (hypertrophy of the distal phalanges), periostosis (subperiosteal new bone ...
N. A. Lyubimova +7 more
doaj +1 more source
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 +1 more source
Reumatismo, 2014 Pachydermoperiostosis is a rare hereditary disorder, which affects both bones and skin. It is characterized by a combination of dermatologic changes (pachydermia or thickening of the skin) and rheumatologic manifestations (periostosis and finger clubbing)
S. El Aoud +4 more
doaj +1 more source
A rare case of pachydermoperiostosis associated with blepharoptosis and floppy eyelids
Indian Journal of Ophthalmology, 2016 Pachydermoperiostosis (PDP) is a multisystem disorder of mesenchymal origin. It is a form of hypertrophic osteoarthropathy. The typical clinical features include pachydermia, cutis verticus gyrata, digital clubbing, and periostosis. Patients present with
Bipasha Mukherjee, Md. Shahid Alam
doaj +1 more source
Giant ectopic liver, hepatocellular carcinoma and pachydermia-a rare genetic syndrome?
Diagnostic Pathology, 2011 Ectopic liver is a very uncommon developmental anomaly that predisposes to the development of hepatocellular carcinoma. We describe the second documented case of a hepatocellular carcinoma developing in the primary liver of a patient with a rare and ...
Miny Peter +5 more
doaj +1 more source
Revista Brasileira de Reumatologia, 2009 A osteoartropatia hipertrófica primária é uma síndrome rara, caracterizada pela presença de baqueteamento digital de mãos e pés, aumento das extremidades e de tecidos periarticulares secundários à proliferação óssea, fisionomia facial grosseira, dor e ...
Aline Biral Zanon +4 more
doaj +1 more source
Reumatismo, 2013 Pachydermoperiostosis as the primary form of hypertrophic osteoarthropathy is a rare hereditary disorder with a number of characteristic findings, e.g. periosteal hypertrophy, digital clubbing and pachydermia.
S. Warwas +3 more
doaj +1 more source