familial combined hyperlipidemia
- familial combined hyperlipidemia
- a genetically heterogeneous, autosomal dominant disorder of lipoprotein metabolism manifest in adulthood as either hypercholesterolemia (type II-a hyperlipoproteinemia phenotype), hypertriglyceridemia (type IV hyperlipoproteinemia phenotype), or a combination (type II-b hyperlipoproteinemia phenotype); different phenotypes may succeed each other in a single individual. The disorder is characterized by greatly elevated plasma apolipoprotein B and premature coronary atherosclerosis, but only occasionally xanthomas. Called also multiple lipoprotein–type h. See also table of hyperlipoproteinemias.
Medical dictionary.
2011.
Look at other dictionaries:
Combined hyperlipidemia — Classification and external resources ICD 10 E78.4 ICD 9 272.4 In medicine … Wikipedia
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
Hyperlipidemia — DiseasesDB = 6255 MeshID = D006949 Hyperlipidemia, hyperlipoproteinemia or dyslipidemia is the presence of raised or abnormal levels of lipids and/or lipoproteins in the blood. Lipids (fatty molecules) are transported in a protein capsule, and… … Wikipedia
multiple lipoprotein–type hyperlipidemia — familial combined h … Medical dictionary
FCHL — familial combined hyperlipidemia … Medical dictionary
FCHL — • familial combined hyperlipidemia … Dictionary of medical acronyms & abbreviations
USF1 — Upstream transcription factor 1, also known as USF1, is a human gene.cite web | title = Entrez Gene: USF1 upstream transcription factor 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=7391| accessdate = ] … Wikipedia
List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… … Wikipedia
TXNIP — Thioredoxin interacting protein, also known as TXNIP, is a human gene.cite web | title = Entrez Gene: TXNIP thioredoxin interacting protein| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=10628| accessdate … Wikipedia
ДЕФЕКТЫ АПОЛИПОПРОТЕИНОВ — мед. Аполипопротеины (апоЛП) белковая часть липопротеинов, формирующих липопротеины высокой плотности (ЛВП), липо протеины низкой плотности (ЛНП), липопротеины очень низкой плотности (ЛОНП) и хиломикроны плазмы. Различают 8 основных типов апоЛП A … Справочник по болезням
