Literature DB >> 10341506

Imerslund-Gräsbeck syndrome in an African patient.

D K Stones1, M Ferreira.   

Abstract

Imerslund-Gräsbeck syndrome (IGS) is a rare cause of megaloblastic anaemia in young children. We wish to report the first case described from Africa. The diagnosis of IGS was made on the findings of a low vitamin B12 level, mild proteinuria, and a vitamin B12 absorption test unaffected by the intrinsic factor. The patient responded well to treatment with intramuscular vitamin B12.

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Year:  1999        PMID: 10341506     DOI: 10.1093/tropej/45.2.106

Source DB:  PubMed          Journal:  J Trop Pediatr        ISSN: 0142-6338            Impact factor:   1.165


  2 in total

1.  Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria.

Authors:  Bugsu Ovunc; Edgar A Otto; Virginia Vega-Warner; Pawaree Saisawat; Shazia Ashraf; Gokul Ramaswami; Hanan M Fathy; Dominik Schoeb; Gil Chernin; Robert H Lyons; Engin Yilmaz; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2011-09-08       Impact factor: 10.121

2.  Imerslund-Grasbeck syndrome in a 5-year-old Iranian boy.

Authors:  K Goudarzipour; N Zavvar; B Behnam; M A Ahmadi
Journal:  Indian J Nephrol       Date:  2016 Nov-Dec
  2 in total

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