Hypercholesterolemia, autosomal dominant

19p13.2, 1q21-q23, 9q22-q31, 8p21-p12, 7p15, 3p21.2-p14.1 Google OMIM Orphanet PubMed [Hypercholesterolemia, familial]

*Gene map locus 19p13.2, 1q21-q23, 9q22-q31, 8p21-p12, 7p15, 3p21.2-p14.1

FHC

Hyperlipoproteinemia, type IIA

LDL receptor disorder

[Clinical features: elevation of serum cholesterol bound to low density lipoprotein; coronary artery disease presenting after age 30 years in heterozygotes, in childhood in homozygotes]

[Inheritance: autosomal dominant]


Heterozygous familial hypercholesterolemia: an underrecognized cause of early cardiovascular disease	Familial hypercholesterolemia with multiple cutaneous xanthomas	Familial hypercholesterolemia with multiple cutaneous xanthomas
Canadian Medical Association Journal	Indian Journal of Dermatology	Indian Journal of Dermatology


Familial hypercholesterolemia with multiple cutaneous xanthomas	Familial hypercholesterolemia with multiple cutaneous xanthomas	Familial hypercholesterolemia with multiple cutaneous xanthomas
Indian Journal of Dermatology	Indian Journal of Dermatology	Indian Journal of Dermatology

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Edited by Aldo Campana, February 8, 2010