A patient with the homozygote form of familial...

A patient with the homozygote form of familial hypercholesterolemia.

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 JW; Schilte PP; Lansberg PJ; Kastelein JJ; Bakker HD

Journal

Tijdschrift Voor Kindergeneeskunde, Vol. 59, No. 3, pp. 88–91

Publication Date

January 1, 1991

ISSN

0376-7442

Associated Experts

Jan Willem Gorter

Professor (Part-Time), Faculty of Health Sciences

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