Pachydermoperiostosis: A case report
| Author | M Banihashemi | en |
| Issued Date | 2002-09-30 | en |
| 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. | en |
| DOI | https://doi.org/ | en |
| Keyword | Primary | en |
| Keyword | Pachydermoperiostosis | en |
| Keyword | Genetic disease | en |
| Publisher | Brieflands | en |
| Title | Pachydermoperiostosis: A case report | en |
| Type | Case Report | en |
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