Abstract
A case of hypertriglyceridemia in association with homozygous β-thalassemia in an 11-month-old female infant is reported. The hypertriglyceridemia proved to be secondary, as it was indicated by clinical features as well as laboratory findings. Attention is called to a possible alteration of lipid metabolism in association with thalassemia major.
Original language | English (US) |
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Pages (from-to) | 83-86 |
Number of pages | 4 |
Journal | Helvetica paediatrica acta |
Volume | 32 |
Issue number | 1 |
State | Published - 1977 |
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health