hyperlipoproteinemia type 1B
Jump to navigation
Jump to search
Etiology
familial apolipoprotein C2 deficiency
Genetics
- autosomal recessive
- associated with defects in APOC2
Clinical manifestations
- clinically indistinguishable from lipoprotein lipase deficiency
Complications
- pancreatitis
- early atherosclerosis
More general terms
References
- ↑ Clinical Diagnosis & Management by Laboratory Methods, J.B. Henry (ed), W.B. Saunders Co., Philadelphia, PA. 1991, pg 208
- ↑ OMIM https://mirror.omim.org/entry/207750