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Pan Afr Med J ; 45: 88, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37663630

RESUMO

Pachydermoperiostosis is a rare genetic disease known as primary or idiopathic hypertrophic osteoarthropathy (HOA)/Touraine-Solente-Gole syndrome. It is an autosomal dominant or recessive disorder comprising digital clubbing, periostosis, hyperhidrosis, and pachydermia (thickening of facial skin). Ocular manifestations are uncommon; however, blepharoptosis may occur. This case presented with severe bilateral ptosis due to the disease progression. A large 20 mm upper lid resection with levator advancement was performed to improve his ability to see. This is the first reported case of pachydermoperiostosis (PDP) in Jamaica. We present a rare case of pachydermoperiostosis with severe blepharoptosis, who attained a good result with surgical intervention.


Assuntos
Blefaroptose , Osteoartropatia Hipertrófica Primária , Humanos , Osteoartropatia Hipertrófica Primária/diagnóstico , Blefaroptose/etiologia , Comorbidade , Face , Olho , Doenças Raras
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