Siddhi Rajesh Patadia, Sunanda Arun Mahajan, Ketki Shekhar Bhoite
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Pachydermoperiostosis is a rare genetic disorder featuring a triad of pachydermia, periostosis and digital clubbing. It is either caused by the mutations in the HPGD (AR inheritance) or SLCO2A1 gene (AD inheritance), resulting in elevated prostaglandins E2 levels. It can be classified on the basis of presence or absence of underlying cardiac, pulmonary or hepatic disease as primary or secondary. We hereby report a case of complete form of primary pachydermoperiostosis.
Bhoite KS, Patadia SR, Mahajan SA, et al. Pachydermoperiostosis, complete form: a case report of rare occurrence. RFP Jr of Drea. 2025;10(2):59-62.
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| Received | Accepted | Published |
|---|---|---|
| May 22, 2025 | September 27, 2025 | December 24, 2025 |
Monday 26 January 2026, 17:33:43 (IST)
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| Received | May 22, 2025 |
| Accepted | September 27, 2025 |
| Published | December 24, 2025 |
This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.