Results 21 to 30 of about 729 (170)

A rare case of pachydermoperiostosis associated with blepharoptosis and floppy eyelids

open access: yesIndian 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   +2 more sources

Arthroscopic synovectomy and radiosynoviorthesis: a treatment option for recurrent arthritis symptoms in patients with pachydermoperiostosis [PDF]

open access: yesReumatismo, 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   +2 more sources

Gastric Juvenile Polyposis with High-Grade Dysplasia in Pachydermoperiostosis

open access: yesCase Reports in Gastroenterology, 2011
Pachydermoperiostosis (PDP) is the primary form of hypertrophic osteoarthropathy. It is a very rare disease consisting of pachydermia, digital clubbing and radiologic periostosis.
L. de Mestier   +5 more
doaj   +2 more sources

Characterization of Mineral and Bone Metabolism Biomarkers in a Chinese Consanguineous Twin Family with Primary Hypertrophic Osteoarthropathy

open access: yesInternational Journal of Endocrinology, 2020
Purpose. Primary hypertrophic osteoarthropathy (PHO) is a rare, autosomal, recessive genetic disease characterized by digital clubbing, periostosis, and pachydermia.
Na Li   +7 more
doaj   +2 more sources

Osteoartropatia hipertrófica idiopática: relato de caso e revisão da literatura Primary hypertrophic osteoarthropathy: case report and literature review

open access: yesRevista 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   +2 more sources

Touraine Solente Gole syndrome: The elephant skin disease

open access: yesIndian 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   +2 more sources

Hypertrophy of the feet and ankles presenting in primary hypertrophic osteoarthropathy or pachydermoperiostosis: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2012
Introduction Pachydermoperiostosis or primary hypertrophic osteoathropathy is a rare genetic disease with autosomal transmission. This disorder, which affects both bones and skin, is characterized by the association of dermatologic changes (pachydermia ...
Akrout Rim   +5 more
doaj   +2 more sources

Interarytenoid Cobblestoning Pachydermia in a Patient With Laryngopharyngeal Reflux [PDF]

open access: yesEar, Nose & Throat Journal, 2022
Chao-Yin Kuo MD   +2 more
doaj   +3 more sources

A case report of an extremely rare association of ankylosing spondylitis with pachydermoperiostosis. [PDF]

open access: yesClin Case Rep, 2023
Key Clinical Message We describe a case of a young man with features of pachydermoperiostosis and spondyloarthropathy. By describing this rarity, we aim to help build a database for future studies and construct a management plan that rheumatologists and clinicians can use.
Gorial FI, Awadh NI, Hamzah MA.
europepmc   +2 more sources

Cutis Verticis Gyrata Across the Diagnostic Spectrum: Two Cases Highlighting Challenges in Clinical Classification. [PDF]

open access: yesClin Case Rep
ABSTRACT Cutis verticis gyrata (CVG) is an uncommon disorder characterized by cerebriform thickening of the scalp that may occur as a primary condition or secondary to a variety of systemic disorders. We report two patients with clinically distinct presentations of CVG illustrating the diagnostic challenges encountered during classification.
Bishokarma S, Acharya SS, Dhami G.
europepmc   +2 more sources

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