Volume 1, Issue 2 (Summer 2013 2013)
Clin Exc 2013, 1(2): 115-119 |
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Karami H, Mohammadjafari H, Roohanizadeh H, Taghipour M. Imerslund-Gräsbeck Syndrome: report of two cases in a family. Clin Exc 2013; 1 (2) :115-119
URL: http://ce.mazums.ac.ir/article-1-55-en.html
URL: http://ce.mazums.ac.ir/article-1-55-en.html
Abstract: (7715 Views)
Imerslund-Gräsbeck Syndrome is an inherited disorder which present as a megaloblastic anemia
followed by selective vitamine B12 deficiency and is associated with mild proteineuria. This rare disease
is easily treatable if detected. In this paper two members of a family with Imerslund-Gräsbeck Syndrome
are reported.
Type of Study: Review |
Subject:
هماتولوژی و انکولوژی کودکان
Received: 2013/08/28 | Accepted: 2013/09/14 | Published: 2013/09/14
Received: 2013/08/28 | Accepted: 2013/09/14 | Published: 2013/09/14
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