Imerslund-Gräsbeck Syndrome: report of two cases in a family
Journal of Clinical Excellence. 2013; 1 (2): 115-122
em Persa
| IMEMR
| ID: emr-177946
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
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Índice:
IMEMR (Mediterrâneo Oriental)
Idioma:
Persa
Revista:
J. Clin. Excell.
Ano de publicação:
2013
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