Acute hypertriglyceridemic pancreatitis during pregnancy due to homozygous lipoprotein lipase gene mutation

Clinica Chimica Acta

Volumn 400, Issue 1-2, 2009, Pages 137-138

  Bartha, Iván ^a   Dinya, Tamás ^a   Seres, Ildikó ^a   Paragh, György ^a   Ross, Colin ^b   Hayden, Michael R ^b   Biró, Sándor ^a   Vargha, György ^a  

^a UNIVERSITY OF DEBRECEN   (Hungary)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CHYLOMICRON; LIPOPROTEIN LIPASE; TRIACYLGLYCEROL; TRYPTOPHAN;

ABDOMINAL ABSCESS; ABDOMINAL PAIN; ACUTE PANCREATITIS; ADULT; BACTERIUM CULTURE; BLOOD SAMPLING; CASE REPORT; DNA SCREENING; ENZYME ACTIVITY; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; GENETIC VARIABILITY; HOMOZYGOSITY; HUMAN; HYDROLYSIS; HYPERLIPOPROTEINEMIA TYPE 1; HYPOCALCEMIA; INTESTINE LAVAGE; JEJUNOSTOMY TUBE; LETTER; LIPOPROTEIN LIPASE GENE; POLYMERASE CHAIN REACTION; PREGNANCY; PRIORITY JOURNAL; SURGICAL TECHNIQUE; TRIACYLGLYCEROL BLOOD LEVEL;

ADULT; FAMILY; FEMALE; HOMOZYGOTE; HUMANS; HYPERTRIGLYCERIDEMIA; LIPOPROTEIN LIPASE; MUTATION; PANCREATITIS; PEDIGREE; PREGNANCY; PREGNANCY COMPLICATIONS;

EID: 57949104788     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cca.2008.10.016     Document Type: Letter

References (10)

1. Henderson H., Leisegang F., Hassan F., Hayden M., and Marais D. A novel Glu421Lys substitution in the lipoprotein lipase gene in pregnancy-induced hypertriglyceridemic pancreatitis. Clin Chim Acta 269 (1998) 1-12
2. Hsia S.H., Connelly P.W., and Hegele R.A. Successful outcome in severe pregnancy-associated hyperlipemia: a case report and literature review. Am J Med Sci 309 (1995) 213-218
3. Murugasu C.G., Armstrong G., Creedon G., Cavanna J.S., Galton D.J., and Tomkin G.H. Acute hypertriglyceridaemic pancreatitis in a pregnant Indian: a new lipoprotein lipase gene mutation. J R Soc Med 91 (1998) 205-207
4. Suga S., Tamasawa N., Kinpara I., et al. Identification of homozygous lipoprotein lipase gene mutation in a woman with recurrent aggravation of hypertriglyceridaemia induced by pregnancy. J Intern Med 243 (1998) 317-321
5. Herrera E. Lipid metabolism in pregnancy and its consequences in the fetus and newborn. Endocrine 19 (2002) 43-55
6. Gagne C., Brun L.D., Julien P., Moorjani S., and Lupien P.J. Primary lipoprotein-lipase-activity deficiency: clinical investigation of a French Canadian population. CMAJ 140 (1989) 405-411
7. Ishimura-Oka K., Faustinella F., Kihara S., Smith L.C., Oka K., and Chan L. A missense mutation (Trp86-Arg) in exon 3 of the lipoprotein lipase gene: a cause of familial chylomicronemia. Am J Hum Genet 50 (1992) 1275-1280
8. Reina M., Brunzell J.D., and Deeb S.S. Molecular basis of familial chylomicronemia: mutations in the lipoprotein lipase and apolipoprotein C-II genes. J Lipid Res 33 (1992) 1823-1832
9. Pasalic D., Jurcic Z., Stipancic G., et al. Missense mutation W86R in exon 3 of the lipoprotein lipase gene in a boy with chylomicronemia. Clin Chim Acta 343 (2004) 179-184
10. Kalmar T., Seres I., Balogh Z., Kaplar M., Winkler G., and Paragh G. Correlation between the activities of lipoprotein lipase and paraoxonase in type 2 diabetes mellitus. Diabetes Metab 31 (2005) 574-580