Title:
An infant with chronic diarrhoea and failure to thrive: Familial hypobetalipoproteinemia

dc.contributor.authorAnkur Singh
dc.contributor.authorRajniti Prasad
dc.contributor.authorOm Prakash Mishra
dc.date.accessioned2026-02-07T06:09:40Z
dc.date.issued2015
dc.description.abstractDiarrhoea is a common clinical problem for treating clinicians in developing countries. Mostly, it is attributed to malnutrition and infection. We, as clinicians, tend to miss some of cases who have inherited enteropathies because of lack of suspicion and non availability of diagnostic facilities. Here, we report a case of homozygous hypobetalipoproteinaemia in a nine-month-old female patient presenting with chronic diarrhoea and failure to thrive. Simple parental screening of lipid parameters led to correct diagnosis and early intervention in present case. © 2015, Journal of Clinical and Diagnostic Research. All Rights Reserved.
dc.identifier.doi10.7860/JCDR/2015/14166.6919
dc.identifier.issn2249782X
dc.identifier.urihttps://doi.org/10.7860/JCDR/2015/14166.6919
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/27178
dc.publisherJournal of Clinical and Diagnostic Research
dc.subjectAbetalipoproteinaemia
dc.subjectAPOB gene
dc.subjectMalnutritio
dc.titleAn infant with chronic diarrhoea and failure to thrive: Familial hypobetalipoproteinemia
dc.typePublication
dspace.entity.typeArticle

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