Publication: Imerslund-Grasbeck Syndrome: A Case Report
| creativeworkseries.issn | ISSN 1990-7974 eISSN 1990-7982 | |
| dc.contributor.author | Ghosh, TN | |
| dc.contributor.author | Nayek, K | |
| dc.contributor.author | Banerjee, A | |
| dc.date.accessioned | 2026-06-01T06:40:53Z | |
| dc.date.available | 2026-06-01T06:40:53Z | |
| dc.date.issued | 2011 | |
| dc.description | TN Ghosh Associate Professor, Department of Paediatrics, Medical College, Burdwan K Nayek Associate Professor, Department of Paediatrics, Medical College, Burdwan A Banerjee Post Graduate Trainee, Department of Paediatrics, Medical College, Burdwan | |
| dc.description.abstract | Abstract: Imerslund-Grasbeck syndrome is a rare autosomal recessive disorder due to selective malabsorption of Vitamin B12 at the level of cobalamin-intrinsic factor receptor mutation in the terminal ileum resulting in megaloblastic anaemia with proteinuria. Early detection of this rare disorder would enable screening and genetic counselling for asymptomatic family members. | |
| dc.identifier | https://doi.org/10.3126/jnps.v31i3.5159 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14572/6318 | |
| dc.language.iso | en_US | |
| dc.publisher | Nepal Paediatric Society (JNPS) | |
| dc.subject | Imerslund Grasbeck Syndrome | |
| dc.subject | Megaloblastic anaemia | |
| dc.subject | Proteinuria | |
| dc.title | Imerslund-Grasbeck Syndrome: A Case Report | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.article.type | Case Report | |
| oaire.citation.endPage | 250 | |
| oaire.citation.startPage | 249 | |
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