Homozygous familial hypercholesterolemia: case report of a rare cause of dyslipidemia Homozygotyczna rodzinna hipercholesterolemia. Opis przypadku dotyczący rzadkich przyczyn dyslipidemii

A 4-year-old boy was evaluated for severe hypercholesterolemia (cholesterol: 831 mg/dL) and disseminated xanthomas. Both parents had hypercholesterolemia: mother (cholesterol: 308 mg/dL) and father (cholesterol: 281 mg/dL). There was no family history of cardiovascular disease. Skin examination show...

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Bibliografische gegevens

Hoofdauteurs:	Cresio Alves, Zilda Braid
Formaat:	Artigo
Taal:	Inglês
Gepubliceerd in:	Termedia Publishing House 2011-09-01
Reeks:	Pediatric Endocrinology, Diabetes and Metabolism
Onderwerpen:	hyperlipoproteinemia type II familial hypercholesterolemia LDL receptor xanthomatosis typu II rodzinna hiperchlesterolemia receptor LDL kępki żółte
Online toegang:	http://cornetis.pl/pliki/ED/2011/3/ED_2011_3_162.pdf
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