Results 51 to 60 of about 1,595 (202)
Pachydermoperiostosis Masquerading as Acromegaly. [PDF]
, 2017 Context: Acromegaly usually is suspected on clinical grounds. Biochemical confirmation is required to optimize therapy, but there are other differential diagnoses.
Cranston, T +5 more
core +1 more source
Pachydermoperiostosis in childhood [PDF]
Rheumatology, 1997 We report a family with pachydermoperiostosis (idiopathic hypertrophic osteoarthropathy) spanning four generations with 10 affected individuals, four of whom are children although pachydermoperiostosis is rare in childhood. In this family, with intermarriage, the inheritance is autosomal recessive and it is possible that there are individuals who are ...
G P, Sinha +5 more
openaire +2 more sources
Clinicopathologic Conference: A Four‐Year‐Old Child With Digital Clubbing
, 2021 Arthritis Care &Research, Volume 73, Issue 10, Page 1379-1386, October 2021.
Katherine Schultz +6 more
wiley +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
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
Elephant skin and droopy lids: A rare case report of touraine-solente-gole syndrome
TNOA Journal of Ophthalmic Science and Research, 2021 Touraine-Solente-Gole syndrome which is also known as pachydermoperiostosis is a multisystem disorder that affects bone, skin including eyelids, gastrointestinal system, and endocrine system.
Rita Hepsi Rani +2 more
doaj +1 more source
Pachydermoperiostosis: a case report
Остеопороз и остеопатии, 2017 Pachydermoperiostosis (PHO) or primary hypertrophic osteoarthropathy is a rare genetic disease that typically begins during childhood or adolescence. It is characterized by digital clubbing, pachydermia and periosteal reaction and progresses gradually ...
Valentina A. Fursenko +3 more
doaj +1 more source
Idiopathic hypertrophic osteoarthropathy misdiagnosed as juvenile idiopathic arthritis. Case study [PDF]
, 2023 Background. Pachydermoperiostosis (or primary hypertrophic osteoarthropathy) is a rare genetic disease that usually begins in childhood or adolescence, is characterized by certain clinical signs (pachydermia, periostosis, drum sticks) that gradually ...
Agachi, Svetlana +4 more
core +1 more source
소아청소년기에서 SLCO2A1 gene 연관 만성 장병증 (CEAS) 의 임상 양상 [PDF]
, 2022 학위논문(석사) -- 서울대학교대학원 : 의과대학 임상의과학과, 2022.2. 고재성.Background and Aims: The incidence of inflammatory bowel disease (IBD) is increasing worldwide, and many atypical IBDs are being discovered.
임진규
core
Differential diagnosis of acromegaly and pachydermoperiostosis
Health and Ecology Issues, 2023 Acromegaly is a neuroendocrine disease with diverse clinical manifestations that develop over a long period. In the process of examining a patient, it may be necessary to conduct a differential diagnosis of acromegaly with various syndromes and ...
N. V. Kholupko +4 more
semanticscholar +1 more source