PACHYDERMOPERIOSTOSIS: A CASE REPORT

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BANIHASHEMI M.

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Journal Paper

Paper Information

Journal: Zahedan Journal of Research in Medical Sciences Year:2002 | Volume:4 | Issue:3 Page(s): 161-164

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Information Journal Paper

Title

PACHYDERMOPERIOSTOSIS: A CASE REPORT

Author(s)

BANIHASHEMI M. | Issue Writer Certificate

Keywords

PRIMARYQ4

PACHYDERMOPERIOSTOSISQ4

GENETIC DISEASEQ4

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.

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APA: Copy

BANIHASHEMI, M.. (2002). PACHYDERMOPERIOSTOSIS: A CASE REPORT. ZAHEDAN JOURNAL OF RESEARCH IN MEDICAL SCIENCES (TABIB-E-SHARGH), 4(3), 161-164. SID. https://sid.ir/paper/84524/en

Vancouver: Copy

BANIHASHEMI M.. PACHYDERMOPERIOSTOSIS: A CASE REPORT. ZAHEDAN JOURNAL OF RESEARCH IN MEDICAL SCIENCES (TABIB-E-SHARGH)[Internet]. 2002;4(3):161-164. Available from: https://sid.ir/paper/84524/en

IEEE: Copy

M. BANIHASHEMI, “PACHYDERMOPERIOSTOSIS: A CASE REPORT,” ZAHEDAN JOURNAL OF RESEARCH IN MEDICAL SCIENCES (TABIB-E-SHARGH), vol. 4, no. 3, pp. 161–164, 2002, [Online]. Available: https://sid.ir/paper/84524/en

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