An Infant with Milky Serum and a Rare Mutation
Indian Pediatr
;
2020 Jan; 57(1): 73-74
Artigo
| IMSEAR
| ID: sea-199459
ABSTRACT
A 40-day-infant having milky serum, eruptive xanthomas,hepatosplenomegaly, lipemia retinalis, high cholesterol andtriglyceride, was found to have lipoprotein lipase (LPL) deficiencyon genetic workup. Triglyceride decreased with dietary fatrestriction, medium chain triglyceride and fibrates.LPLdeficiency in early infancy can be treated with pharmacologicaland dietary interventions.
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IMSEAR (Sudeste Asiático)
Revista:
Indian Pediatr
Ano de publicação:
2020
Tipo de documento:
Artigo
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