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hyperlipoproteinemia type 1B

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

General

hyperlipoproteinemia type 1; familial hyperchylomicronemia

Database Correlations

OMIM 207750

References

  1. Clinical Diagnosis & Management by Laboratory Methods, J.B. Henry (ed), W.B. Saunders Co., Philadelphia, PA. 1991, pg 208
  2. OMIM :accession 207750