ArticleClinical case reports2019
Complete primary pachydermoperiostosis: A case report from Jordan and review of literature.
Article in Clinical case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed.
- Cutis Verticis Gyrata Across the Diagnostic Spectrum: Two Cases Highlighting Challenges in Clinical Classification.Clinical case reports · 2026Article
- From Juvenile Idiopathic Arthritis to Pachydermoperiostosis: A Journey to an Unexpected Rare Diagnosis.Journal of clinical medicine · 2026Article
- Pachydermoperiostosis Due to a NovelJCEM case reports · 2024Article
- Clinical Outcomes of Utilizing a "W"-shaped Incision in the Management of Forehead Skin Thickening Induced by Hypertrophic Osteoarthropathy.Aesthetic plastic surgery · 2024Article
- Article
- Reclassification of theCold Spring Harbor molecular case studies · 2023Article
- Identification of three novel mutations inThe Indian journal of medical research · 2023Article
- Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from TurkeyJournal of clinical research in pediatric endocrinology · 2022Article
- Familial Touraine-Solente-Gole syndrome.BMJ case reports · 2022Article
- A Case of Progressive Thickening and Furrowing of Facial Skin and Scalp with Scarring Alopecia.Skin appendage disorders · 2021Article
- Frontal lifting using a tissue expander in pachydermoperiostosis: A case report.Clinical case reports · 2021Article
- Complete primary pachydermoperiostosis: A case report from Jordan and review of literature.Clinical case reports · 2019Article
- Comprehensive Treatment of a Rare Case of Complete Primary Pachydermoperiostosis with Large Facial Keloid Scars: A Case Report and Literature Review.Case reports in dermatologyArticle
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Complete Primary Pachydermoperiostosis is a rare syndrome that presents with skin and skeletal manifestations. Though diagnosis can be made on the basis of the classic clinical and radiological features, it is often missed due to variable presentations. Therefore, it is important to know about this syndrome to reach correct diagnosis.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.