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Published in 2021 at "Journal of Ayurveda and Integrative Medicine"
DOI: 10.1016/j.jaim.2021.08.010
Abstract: Hypertriglyceridemia is a rare disorder in childhood. Familial Chylomicronemia Syndrome (FCS) is a rare genetic disease that leads to severe hypertriglyceridemia, often associated with recurrent episodes of pancreatitis. In this syndrome, traditional lipid-lowering drugs are…
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Keywords:
recurrent episodes;
management infant;
medicine;
ayurveda management ... See more keywords
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Published in 2024 at "BMC Anesthesiology"
DOI: 10.1186/s12871-024-02812-2
Abstract: The syndrome has these features: 3-methylglutaconic aciduria (MEG), deafness(D), encephalopathy (E), Leigh-like syndrome (L). This disorder is caused by biallelic mutations in serine active site-containing protein 1 (SERAC1) gene. When these patients experience hepatopathy (H)…
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Keywords:
pathology;
anaesthetic management;
management infant;
megd syndrome ... See more keywords