See Also: familial hyperchylomicronaemia(medicine)
familial hyperchylomicronaemia with hyperprebetalipoproteinaemia(medicine)
EXONERATUR, practice(law)
hyperchylomicronaemia(medicine)
Familial ALS(health)
familial(dictionary)
familial(dictionary)
Familial(medicine)
Familial(health)
familial lipodystrophy(medicine)

EXONERATUR, practice (law) and familial hyperchylomicronaemia (medicine)


EXONERATUR, practice (law)


EXONERATUR, practice. A short note entered on a bail piece, that the bail is exonerated or discharged in consequence of having fulfilled the condition of exonerated or discharged in consequence of having fulfilled the condition of his obligation, made by order of the court or of a judge upon a proper cause his obligation, made by order of the court or of a judge upon a proper cause being shown. being shown. 2. A surrender is the most usual cause; but an exoneratur may be 2. A surrender is the most usual cause; but an exoneratur may be entered in Other cases, as in case of death of the defendant, or his entered in Other cases, as in case of death of the defendant, or his bankruptcy. 1 Arch. Pr. 280, 281, 282; Tidd' s Pr. 240. bankruptcy. 1 Arch. Pr. 280, 281, 282; Tidd' s Pr. 240.

familial hyperchylomicronaemia (medicine)


familial hyperchylomicronaemia -->
type I familial hyperlipoproteinaemia
Hyperlipoproteinaemia characterised by the presence of large amounts of chylomicrons and triglycerides in the plasma when the patient has a normal diet, and their disappearance on a fat-free diet; low alpha-and beta-lipoproteins on a normal diet, with increase on fat-free diet; decreased plasma postheparin lipolytic activity; and low tissue lipoprotein lipase activity. It is accompanied by bouts of abdominal pain, hepatosplenomegaly, pancreatitis, and eruptive xanthomas; autosomal recessive inheritance.

See: familial lipoprotein lipase inhibitor.

Synonym: Burger-Grutz syndrome, familial fat-induced hyperlipaemia, familial hyperchylomicronaemia, familial hypertriglyceridemia, idiopathic hyperlipaemia.