REVIEW: IMERSLUND-GRASBECK SYNDROME: REPORT OF TWO CASES IN A FAMILY

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KARAMI HOSSEIN; MOHAMMADJAFARI HAMID; ROOHANIZADEH HAMED; TAGHIPOUR MEHRDAD

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Journal: JOURNAL OF CLINICAL EXCELLENCE Year:2013 | Volume:1 | Issue:2 Page(s): 115-119

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Information Journal Paper

Title

REVIEW: IMERSLUND-GRASBECK SYNDROME: REPORT OF TWO CASES IN A FAMILY

Author(s)

KARAMI HOSSEIN | MOHAMMADJAFARI HAMID | ROOHANIZADEH HAMED | TAGHIPOUR MEHRDAD | Issue Writer Certificate

Keywords

MEGALOBLASTIC ANEMIAQ2

IMERSLUND-GRASBECK SYNDROMEQ2

PROTEINEURIAQ3

Abstract

Imerslund-Grasbeck 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-GRASBECK SYNDROME are reported.

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APA: Copy

KARAMI, HOSSEIN, MOHAMMADJAFARI, HAMID, ROOHANIZADEH, HAMED, & TAGHIPOUR, MEHRDAD. (2013). REVIEW: IMERSLUND-GRASBECK SYNDROME: REPORT OF TWO CASES IN A FAMILY. JOURNAL OF CLINICAL EXCELLENCE, 1(2), 115-119. SID. https://sid.ir/paper/243959/en

Vancouver: Copy

KARAMI HOSSEIN, MOHAMMADJAFARI HAMID, ROOHANIZADEH HAMED, TAGHIPOUR MEHRDAD. REVIEW: IMERSLUND-GRASBECK SYNDROME: REPORT OF TWO CASES IN A FAMILY. JOURNAL OF CLINICAL EXCELLENCE[Internet]. 2013;1(2):115-119. Available from: https://sid.ir/paper/243959/en

IEEE: Copy

HOSSEIN KARAMI, HAMID MOHAMMADJAFARI, HAMED ROOHANIZADEH, and MEHRDAD TAGHIPOUR, “REVIEW: IMERSLUND-GRASBECK SYNDROME: REPORT OF TWO CASES IN A FAMILY,” JOURNAL OF CLINICAL EXCELLENCE, vol. 1, no. 2, pp. 115–119, 2013, [Online]. Available: https://sid.ir/paper/243959/en

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