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Transient infantile hypertriglyceridemia with jaundice: A case report
RATIONALE: Transient infantile hypertriglyceridemia (HTGTI) is a rare autosomal recessive inherited disease caused by inactivating mutations in the glycerol-3-phosphate dehydrogenase 1 gene. To date, only a few patients have been reported worldwide. The symptoms of the affected individuals present a...
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| Vydáno v: | Medicine (Baltimore) |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Lippincott Williams & Wilkins
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8084070/ https://ncbi.nlm.nih.gov/pubmed/33907148 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000025697 |
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