Rothmund-Thomson Syndrome Associated with Malignant Fibrous Histiocytoma: Report of a Case and Review of Literature

Background: Rothmund–Thomson syndrome is a rare autosomal recessive genodermatosis characterized by the early onset of poikiloderma, and several other cutaneous layers and organ involvements. Case Report: This is a report of a 14-year-old girl who has been diagnosed with Rothmund–Thomson syndrome si...

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Bibliographic Details
Main Authors: Mir Hadi Aziz Jalali, Mehdi Tabaie
Format: Article
Language:fas
Published: Vesnu Publications 2012-03-01
Series:مجله دانشکده پزشکی اصفهان
Subjects:
Online Access:http://jims.mui.ac.ir/index.php/jims/article/view/1728