Familial hypercholesterolemia associated with severe hypoalphalipoproteinemia in a Moroccan family

J Genet. 2007 Aug;86(2):159-63. doi: 10.1007/s12041-007-0020-0.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apolipoprotein A-I / genetics
  • Apolipoproteins B / genetics
  • Apolipoproteins E / genetics
  • DNA Mutational Analysis
  • Family
  • Glucosylceramidase / genetics
  • Humans
  • Hyperlipoproteinemia Type II / complications*
  • Hyperlipoproteinemia Type II / genetics*
  • Hypoalphalipoproteinemias / complications*
  • Hypoalphalipoproteinemias / genetics*
  • Lipoprotein Lipase / genetics
  • Male
  • Morocco
  • Pedigree
  • Phosphatidylcholine-Sterol O-Acyltransferase / genetics
  • Polymorphism, Single Nucleotide
  • Receptors, LDL / genetics

Substances

  • Apolipoprotein A-I
  • Apolipoproteins B
  • Apolipoproteins E
  • Receptors, LDL
  • Phosphatidylcholine-Sterol O-Acyltransferase
  • Lipoprotein Lipase
  • Glucosylceramidase