Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis
Pachydermoperiostosis, or primary hypertrophic osteoarthropathy (PHO), is an inherited multisystem disorder, whose features closely mimic the reactive osteoarthropathy that commonly accompanies neoplastic and inflammatory pathologies.
A. Superti-Furga +107 more
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Pachydermoperiostosis with bilateral ptosis and its associated systemic comorbidities: a rare case report. [PDF]
Hlaing SS +8 more
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A rare case of pachydermoperiostosis associated with blepharoptosis and floppy eyelids
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
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Pachydermoperiostosis and Work Restrictions: A Case Report. [PDF]
Chinichian M +3 more
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Pachydermoperiostosis: a case report of initial improvement with etoricoxib. [PDF]
Vaidya N +4 more
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I, Hassan +3 more
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Identification of three novel mutations in <i>SLCO2A1</i> in Asian-Indians with Pachydermoperiostosis. [PDF]
Pasumarthi D +5 more
europepmc +1 more source
Pachydermoperiostosis (Touraine-Solente-Gole syndrome): A case report and literature review. [PDF]
Hu X, Li M, Li M, Zhou Z.
europepmc +1 more source
Acquired digital clubbing in 2 healthy young men: The incomplete form of pachydermoperiostosis (primary hypertrophic osteoarthropathy). [PDF]
Staunton MK, Chang MW.
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A rare clinical image of pachydermoperiostosis (Touraine-Solente-Gole syndrome). [PDF]
Joshi T, Patharkar J.
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