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Complete form of pachydermoperiostosis in a 16-year-old boy: A case report

Pachydermoperiostosis is an inherited osseocutaneous disorder. The unusual increased levels of prostaglandin E2 due to mutations in either HPGD gene or SLCO2A1 gene are regarded as the causative factor. Our case report is about a 16-year-old boy who presented with cutis verticis gyrata, clubbing of...

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Bibliographic Details
Main Authors:	Sahana M Srinivas (Author), Suman Swamynathan (Author), Vani Hebbal Nagarajappa (Author), Raghupathy Palany (Author)
Format:	Book
Published:	Wolters Kluwer Medknow Publications, 2022-01-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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