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Zahedan Journal of Research in Medical Sciences
The Official Journal of Zahedan University of Medical Sciences
e-ISSN 2383-2894
Outline
Pachydermoperiostosis: A case report
Authors
1Dermatology Dept, faculty of medicine , Zahedan university of medical sciences and health services, Zahedan, Iran.
*Corresponding Author: Dermatology Dept, faculty of medicine , Zahedan university of medical sciences and health services, Zahedan, Iran. Email: [email protected]
Published online:Sep 26, 2002
Article type:Case Report
Received:Sep 01, 2002
Accepted:Sep 16, 2002
How to Cite:Banihashemi M. Pachydermoperiostosis: A case report. Zahedan J Res Med Sci. 2002;4(3):e95320. doi:
Abstract
Primary Pachydermoperiostosis is a rare hereditary disease characterized by folded coarse
skin, hyperostosis, clubbing and abnormality in other organ such as gastrointestinal tract.
This syndrome is autosomal dominant with variable expressivity, but a family with autosomal
recessive had also been reported. Disease occurs predominantly in men. Secondary form is
usually a provoked by sever pulmonary disease. Treatment is symptomatic. This is a case report
of such patient from Baloochestan, Iran.
References
- 1.The References of this article are available on the PDF file.
Copyright
© 2002, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
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