[A patient with the homozygote form of familial hypercholesterolemia]. Journal Articles

abstract

• The history of an 11 year old boy with homozygous familial hypercholesterolemia with therapeutic response to cholesterol lowering drugs is presented. Symptoms, laboratory diagnosis and therapeutic problems are discussed.

authors

• Gorter, Jan Willem
• Schilte, PP
• Lansberg, PJ
• Kastelein, JJ
• Bakker, HD

status

• published 

publication date

• June 1991

has subject area

• Anticholesteremic Agents (MeSH)
• Child (MeSH)
• Exercise Test (MeSH)
• Homozygote (MeSH)
• Humans (MeSH)
• Hydroxymethylglutaryl-CoA Reductase Inhibitors (MeSH)
• Hyperlipoproteinemia Type II (MeSH)
• Lipoproteins (MeSH)
• Lovastatin (MeSH)
• Male (MeSH)
• Pediatrics (Science Metrix)
• Simvastatin (MeSH)
• Triglycerides (MeSH)

published in

• Tijdschrift voor Kindergeneeskunde  Journal

keywords

• Anticholesteremic Agents
• Child
• Exercise Test
• Homozygote
• Humans
• Hydroxymethylglutaryl-CoA Reductase Inhibitors
• Hyperlipoproteinemia Type II
• Lipoproteins
• Lovastatin
• Male
• Simvastatin
• Triglycerides

PubMed ID

• 1862513

start page

• 88

end page

• 91

volume

• 59

issue

• 3