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Unusual Cause of Childhood Anemia: Imerslund Grasbeck Syndrome
Imerslund Grasbeck syndrome (IGS) is a rare autosomal recessive childhood disorder characterized by selective Vitamin (vit) B 12 malabsorption with asymptomatic proteinuria without any structural renal pathology. The patients stay healthy for decades with life-long parenteral vit B12. We report a ca...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249707/ https://www.ncbi.nlm.nih.gov/pubmed/22219566 http://dx.doi.org/10.4103/0974-2727.86845 |
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author | Laxminarayana, Kishan Prasad Hosapatna Yeshvanth, Sunil Kumar Shetty, Jayaprakash K Permi, Harish S Rao, Chandrika |
author_facet | Laxminarayana, Kishan Prasad Hosapatna Yeshvanth, Sunil Kumar Shetty, Jayaprakash K Permi, Harish S Rao, Chandrika |
author_sort | Laxminarayana, Kishan Prasad Hosapatna |
collection | PubMed |
description | Imerslund Grasbeck syndrome (IGS) is a rare autosomal recessive childhood disorder characterized by selective Vitamin (vit) B 12 malabsorption with asymptomatic proteinuria without any structural renal pathology. The patients stay healthy for decades with life-long parenteral vit B12. We report a case of young female who presented with pancytopenia and proteinuria, evaluated in local hospitals as chronic hemolytic anemia (autoimmune cause), finally diagnosed as IGS on complete evaluation. She was treated with injectable vit B12 (1000 μg cyanocobalalmin) and showed drastic recovery. IGS should be considered in patients with megaloblastic anemia not responding to oral vit B12 and associated proteinuria. |
format | Online Article Text |
id | pubmed-3249707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32497072012-01-04 Unusual Cause of Childhood Anemia: Imerslund Grasbeck Syndrome Laxminarayana, Kishan Prasad Hosapatna Yeshvanth, Sunil Kumar Shetty, Jayaprakash K Permi, Harish S Rao, Chandrika J Lab Physicians Case Report Imerslund Grasbeck syndrome (IGS) is a rare autosomal recessive childhood disorder characterized by selective Vitamin (vit) B 12 malabsorption with asymptomatic proteinuria without any structural renal pathology. The patients stay healthy for decades with life-long parenteral vit B12. We report a case of young female who presented with pancytopenia and proteinuria, evaluated in local hospitals as chronic hemolytic anemia (autoimmune cause), finally diagnosed as IGS on complete evaluation. She was treated with injectable vit B12 (1000 μg cyanocobalalmin) and showed drastic recovery. IGS should be considered in patients with megaloblastic anemia not responding to oral vit B12 and associated proteinuria. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3249707/ /pubmed/22219566 http://dx.doi.org/10.4103/0974-2727.86845 Text en Copyright: © Journal of Laboratory Physicians http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Laxminarayana, Kishan Prasad Hosapatna Yeshvanth, Sunil Kumar Shetty, Jayaprakash K Permi, Harish S Rao, Chandrika Unusual Cause of Childhood Anemia: Imerslund Grasbeck Syndrome |
title | Unusual Cause of Childhood Anemia: Imerslund Grasbeck Syndrome |
title_full | Unusual Cause of Childhood Anemia: Imerslund Grasbeck Syndrome |
title_fullStr | Unusual Cause of Childhood Anemia: Imerslund Grasbeck Syndrome |
title_full_unstemmed | Unusual Cause of Childhood Anemia: Imerslund Grasbeck Syndrome |
title_short | Unusual Cause of Childhood Anemia: Imerslund Grasbeck Syndrome |
title_sort | unusual cause of childhood anemia: imerslund grasbeck syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249707/ https://www.ncbi.nlm.nih.gov/pubmed/22219566 http://dx.doi.org/10.4103/0974-2727.86845 |
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