A Report of Two Cases of Rud Syndrome
Rud syndrome is a rare disease entity that consists of congenital ichthyosis, mental retardation, hypogonadism, and epilepsy. In this article two cases that are sibling are reported. The parents are relative. The elder one who is a 16-yr old female suffers from sever ichthyosis, hypocalcemic tetany,...
Main Authors: | , |
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Format: | Article |
Language: | fas |
Published: |
Hamadan University of Medical Sciences
2000-03-01
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Series: | پزشکی بالینی ابن سینا |
Subjects: | |
Online Access: | http://sjh.umsha.ac.ir/article-1-1013-en.html |