An Infant with Milky Serum and a Rare Mutation
Indian Pediatr
;
2020 Jan; 57(1): 73-74
Article
| 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.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Texte intégral:
Indian Pediatr
Année:
2020
Type:
Article
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