Publication:
Hypopituitarism: A Very Rare Cause of Dilated Cardiomyopathy in a Child

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorMandal, Anirban
dc.contributor.authorSingh, Amitabh
dc.date.accessioned2026-02-05T09:57:38Z
dc.date.available2026-02-05T09:57:38Z
dc.date.issued2017
dc.descriptionAnirban Mandal Attending Consultant, Department of Paediatrics, Sitaram Bhartia Instiute of Science and Research, New Delhi Amitabh Singh Assistant Professor, Department of Paediatrics, VMMC and Safdarjung Hospital, New Delhi http://orcid.org/0000-0002-4440-5339
dc.description.abstractAbstract: Dilated cardiomyopathy (DCMP), the leading type of cardiomyopathy in children, can be either a primary disease or secondary to a host of pathologies. Endocrine diseases are an extremely rare cause of DCMP in children. Hypopituitarism (congenital or acquired), a rare condition in children, may present in a variety of phenotypes depending on the hormonal deficiency (partial vs. pan hypopituitarism) and associated developmental defects. We describe a 10 year old boy with short stature, severely retarded bone age and congestive cardiac failure (CCF). He was diagnosed to have DCMP with hypopituitarism. Review of literature reveal possible mechanisms of DCMP and CCF in hypopituitarism and probably also indicate favorable response to hormonal replacement therapy.
dc.identifierhttps://doi.org/10.3126/jnps.v37i2.17278
dc.identifier.urihttps://hdl.handle.net/20.500.14572/4539
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectCongestive cardiac failure
dc.subjectpericardial effusion
dc.subjectshort stature
dc.subjecthypoglycemia
dc.titleHypopituitarism: A Very Rare Cause of Dilated Cardiomyopathy in a Child
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage200
oaire.citation.startPage197
relation.isJournalIssueOfPublication74bfc0ad-607d-4af9-8e02-dcded43c4176
relation.isJournalIssueOfPublication.latestForDiscovery74bfc0ad-607d-4af9-8e02-dcded43c4176
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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