Imerslund-Gräsbeck Syndrome: report of two cases in a family

Karami, Hossein and Mohammadjafari, Hamid and Roohanizadeh, Hamed and Taghipour, Mehr (2013) Imerslund-Gräsbeck Syndrome: report of two cases in a family. Clinical Excellence, 1 (2). pp. 115-119.

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Official URL: http://ce.mazums.ac.ir/article-1-55-en.html

Abstract

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.

Item Type: Article
Uncontrolled Keywords: Megaloblastic anemia, Imerslund-Gräsbeck Syndrome, Proteineuria
Depositing User: Unnamed user with email eprints@mazums.ac.ir
Date Deposited: 04 Jan 2018 17:08
Last Modified: 04 Jan 2018 17:08
URI: http://eprints.mazums.ac.ir/id/eprint/2715

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