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・ Familial amyloid cardiomyopathy
・ Familial amyloid neuropathy
・ Familial aortic dissection
・ Familial atrial fibrillation
・ Familial British dementia
・ Familial cirrhosis
・ Familial dysalbuminemic hyperthyroxinemia
・ Familial dysautonomia
・ Familial dysbetalipoproteinemia
・ Familial encephalopathy with neuroserpin inclusion bodies
・ Familial exudative vitreoretinopathy
・ Familial hemiplegic migraine
・ Familial homicide
・ Familial hyperaldosteronism
・ Familial hypercholesterolemia
Familial hypertriglyceridemia
・ Familial hypocalciuric hypercalcemia
・ Familial isolated vitamin E deficiency
・ Familial male-limited precocious puberty
・ Familial Mediterranean fever
・ Familial multiple intestinal atresia
・ Familial myxovascular fibromas
・ Familial partial lipodystrophy
・ Familial progressive hyperpigmentation
・ Familial renal amyloidosis
・ Familial renal disease in animals
・ Familial thoracic aortic aneurysm
・ Familialism
・ Familianten
・ Familiar (disambiguation)


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Familial hypertriglyceridemia : ウィキペディア英語版
Familial hypertriglyceridemia
Familial hypertriglyceridemia is an autosomal dominant condition occurring in approximately 1% of the population.〔Boman H,Hazzard WR, AlbersJJ, et ah Frequency of monogenic forms of hyperlipidemia in a normal population. AmJ ttum Genet 27:19A,1975. ()〕 Triglyceride levels, but not cholesterol, are elevated as a result of excess hepatic production of VLDL or heterozygous LPL deficiency. Unlike familial hypercholesterolemia, there is no association with premature coronary disease. However, affected individuals are at risk for chylomicronemia syndrome, characterized by elevated chylomicrons in the blood.
== See also ==

* Primary hyperlipoproteinemia
* Familial apoprotein CII deficiency
* Skin lesion

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