Literature DB >> 23105777

An unusual case of familial hyperlipidaemia.

Renu Nagar1, Uma Arora.   

Abstract

A 40 days old male baby born to a consanguineous couple was found to have highly viscous and milky serum with caking of chylomicrons on refrigeration of serum. Cholesterol was 889.5 mg/dl (23.04mmol/L) and Triglycerides 12881 mg/dl (141.69mmol/L). He was active and did not have any hepatospleenomegaly, xanthomas or dysmorphic features. Thyroid functions were normal. Lipid electrophoresis showed thick chylomicron band. There was positive family history of hypertriglyceridemia in a first cousin. Both siblings and both parents of the index case had normal lipid profiles. This child was referred to higher centre where he was put on Lipid lowering drugs (Gemfibrozil), Iron drops and special formula for feeding containing medium chain fatty acids.

Entities:  

Keywords:  Hypertriglyceridemia; Lipid lowering drugs; Xanthomas

Year:  2008        PMID: 23105777      PMCID: PMC3453435          DOI: 10.1007/s12291-008-0069-4

Source DB:  PubMed          Journal:  Indian J Clin Biochem        ISSN: 0970-1915


  5 in total

1.  Familial chylomicronemia syndrome.

Authors:  M K Mohandas; J Jemila; A S Ajith Krishnan; T Thomas George
Journal:  Indian J Pediatr       Date:  2005-02       Impact factor: 1.967

2.  An unusual case of severe hypertriglyceridemia and splenomegaly.

Authors:  Amit R Rahalkar; Jian Wang; Sandra Sirrs; James Dimmick; Daniel Holmes; Nadine Urquhart; Robert A Hegele; Andre Mattman
Journal:  Clin Chem       Date:  2008-03       Impact factor: 8.327

3.  Molecular basis of familial chylomicronemia: mutations in the lipoprotein lipase and apolipoprotein C-II genes.

Authors:  M Reina; J D Brunzell; S S Deeb
Journal:  J Lipid Res       Date:  1992-12       Impact factor: 5.922

4.  The 16-hour-standing test and lipoprotein electrophoresis compared for detection of chylomicrons in plasma.

Authors:  S McNeely; K Seatter; J Yuhaniak; M L Kashyap
Journal:  Clin Chem       Date:  1981-05       Impact factor: 8.327

5.  Detection of mutations in the apolipoprotein CII gene by denaturing gradient gel electrophoresis. Identification of the splice site variant apolipoprotein CII-Hamburg in a patient with severe hypertriglyceridemia.

Authors:  M S Nauck; H Nissen; M M Hoffmann; J Herwig; C R Pullinger; M Averna; J Geisel; H Wieland; W März
Journal:  Clin Chem       Date:  1998-07       Impact factor: 8.327

  5 in total
  3 in total

1.  An infant with milky blood : an unusual but treatable case of familial hyperlipidemia.

Authors:  Om Shankar Chaurasiya; Lalit Kumar; Rohit Shamsher Sethi
Journal:  Indian J Clin Biochem       Date:  2012-12-11

2.  Two siblings with familial chylomicronemia syndrome: disease course and effectiveness of early treatment.

Authors:  Hanan Al Azkawi; Ibrahim Alalwan
Journal:  Case Rep Med       Date:  2010-12-27

3.  Neonatal hyperlipidemia with pancreatitis: Novel gene mutation of lipoprotein lipase.

Authors:  M H Shah; R Roshan; R Desai; S S Kadam
Journal:  J Postgrad Med       Date:  2018 Oct-Dec       Impact factor: 1.476

  3 in total

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