Publication:
Transient Non-Ketotic Hyperglycinemia in a Newborn

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorChoudhury, Tarak
dc.contributor.authorKundu,Soumi
dc.contributor.authorDas, G.C.
dc.contributor.authorDasgupta, Malay Kumar
dc.date.accessioned2026-02-23T09:33:35Z
dc.date.available2026-02-23T09:33:35Z
dc.date.issued2016
dc.descriptionTarak Choudhury RG Kar Medical College, Kolkata, West Bengal Soumi Kundu RG Kar Medical College, Kolkata, West Bengal G.C. Das RG Kar Medical College, Kolkata, West Bengal Malay Kumar Dasgupta RG Kar Medical College, Kolkata, West Bengal
dc.description.abstractAbstract: In encephalopathic infants, cerebrospinal fluid hyperglycinemia and elevated cerebrospinal fluid to plasma glycine ratio are considered pathognomonic of Non-ketotic hyperglycinemia (NKH). It is due to a defect of the glycine cleavage system and has poor prognosis. We present a case of transient NKH presented to us with hypotonia, recurrent apnea and seizure. Increased ratio of cerebrospinal fluid to plasma glycine concentrations of 0.16 was seen as a strong diagnostic indicator of Non-ketotic hyperglycinemia.
dc.identifierhttps://doi.org/10.3126/jnps.v36i3.16047
dc.identifier.urihttps://hdl.handle.net/20.500.14572/4876
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectNKH
dc.subjectapnea
dc.subjectseizures
dc.subjecthypotonia
dc.subjectglycine
dc.subjectCSF
dc.subjectplasma
dc.titleTransient Non-Ketotic Hyperglycinemia in a Newborn
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage306
oaire.citation.startPage303
relation.isJournalIssueOfPublication0692fd39-d464-4878-b0ff-743d5b445183
relation.isJournalIssueOfPublication.latestForDiscovery0692fd39-d464-4878-b0ff-743d5b445183
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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