Volume 1, Issue 2 (Summer 2013 2013)                   Clin Exc 2013, 1(2): 115-119 | Back to browse issues page

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Imerslund-Gräsbeck Syndrome: report of two cases in a family
Hossein Karami , Hamid Mohammadjafari , Hamed Roohanizadeh , Mehrdad Taghipour
Abstract:   (8872 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.
Keywords: Megaloblastic anemia, Imerslund-Gräsbeck Syndrome, Proteineuria
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Type of Study: Review | Subject: هماتولوژی و انکولوژی کودکان
Received: 2013/08/28 | Accepted: 2013/09/14 | Published: 2013/09/14
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