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Article

Familial Hyperchylomicronemia Syndrome in a Term Neonate.

Annals of African medicine - 1 Aug 2026

Kumar Sudesh, Priyadarshi Avinash, Sanjay Soumya

Abstract excerpt

ABSTRACT: Familial hyperchylomicronemia syndrome, which is also known as type 1 hyperlipoproteinemia, is a very rare autosomal recessive disorder of lipoprotein metabolism which affects approximately one per million individuals. Familial hyperchylomicronemia is characterized by severe hypertriglyceridemia,with triglyceride level>880 mg/L. This is result of excessive accumulation of chylomicron and inherited...

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Identifiers

PMID: 41778478
DOI: 10.4103/aam.aam_624_25

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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