familial high-density lipoprotein deficiency

familial high-density lipoprotein deficiency
any of several inherited disorders of lipoprotein and lipid metabolism that result in decreased plasma levels of high-density lipoproteins, particularly Tangier disease.

Medical dictionary. 2011.

Игры ⚽ Нужна курсовая?

Look at other dictionaries:

  • deficiency — An insufficient quantity of some substance (as in dietary d. or hemoglobin d. in marrow aplasia); organization (as in mental d.); activity (as in enzyme d. or reduced oxygen carrying capacity of the blood), etc., of which the amount present is of …   Medical dictionary

  • Familial hypercholesterolemia — Classification and external resources Xanthelasma palpebrarum, yellowish patches consisting of cholesterol deposits above the eyelids. These are more common in people with FH. ICD …   Wikipedia

  • Lipoprotein(a) — (also called Lp(a)) is a lipoprotein subclass. Studies have identified Lp(a) as a putative risk factor for atherosclerotic diseases such as coronary heart disease and stroke.cite journal | author = Danesh J, Collins R, Peto R | title =… …   Wikipedia

  • Lipoprotein-X — (Lp X) is an abnormal low density lipoprotein found in cholestasis. Structure Lipoprotein X is a lamellar particle of 30 to 70 nm in diameter as revealed by electron microscopy. It is characterized by its high content of phospholipids (66% by… …   Wikipedia

  • familial hypercholesterolemia — Pathol. an inherited metabolic disorder caused by a lack or malfunction of receptors for the low density lipoproteins that activate removal of cholesterol from the blood. Abbr.: FH. * * * ▪ medical disorder  an inherited metabolic disease that is …   Universalium

  • analphalipoproteinemia — High density lipoprotein deficiency; a heritable disorder of lipid metabolism characterized by almost complete absence from plasma of high density lipoproteins, and by storage of cholesterol esters in foam cells, tonsillar …   Medical dictionary

  • Familiäre Hypoalphalipoproteinämie — Klassifikation nach ICD 10 E78.6 Lipoproteinmangel Tangier Krankheit E75.6 systematisierte Lipidablagerungserkrankung …   Deutsch Wikipedia

  • Hypoalphalipoproteinämie — Klassifikation nach ICD 10 E78.6 Lipoproteinmangel Tangier Krankheit E75.6 systematisierte Lipidablagerungserkrankung …   Deutsch Wikipedia

  • Tangierkrankheit — Klassifikation nach ICD 10 E78.6 Lipoproteinmangel Tangier Krankheit E75.6 systematisierte Lipidablagerungserkrankung …   Deutsch Wikipedia

  • Donald S. Fredrickson — Donald S. Fredrickson, 1961 Donald S. Fredrickson (* 8. August 1924 in Cañon City; † 7. Juni 2002 in Bethesda, Maryland[1]) war Physiologe und beschrieb 1961 als erster die …   Deutsch Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”