Pancreatic triacylglycerol lipase deficiency
ORPHA:309031· ICD-10 K90.3
Definition
A rare genetic disorder of lipid metabolism characterized by neonatal to childhood onset of impaired absorption of dietary fat with greasy/oily and voluminous stools, but normal growth and development. Decreased levels of fecal elastase, as well as low serum levels of the fat-soluble vitamins A, D, and E, have been reported.
- Prevalence
- Unknown
- Inheritance
- Not applicable
- Age of onset
- Infancy