homozygous familial hypercholesterolemia

См. также в других словарях:

• 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

• 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

• HoFH — homozygous familial hypercholesterolemia …   Medical dictionary

• HoFH — • homozygous familial hypercholesterolemia …   Dictionary of medical acronyms & abbreviations

• Orphan drug — An orphan drug is a pharmaceutical agent that has been developed specifically to treat a rare medical condition, the condition itself being referred to as an orphan disease. The assignment of orphan status to a disease and to any drugs developed… …   Wikipedia

• Lipidapherese — Die Lipidapherese ist ein extrakorporales Blutreinigungsverfahren zur Entfernung von LDL Cholesterin und weiteren Faktoren der Arteriosklerose wie Lipoprotein(a) und Triglyzeriden aus dem Blut. Die Lipidapherese wird bei Patienten eingesetzt, die …   Deutsch Wikipedia

• Sitosterolemia — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29796 ICD10 = ICD9 = ICDO = OMIM = 210250 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 2110 MeshID = Sitosterolemia (also known as phytosterolemia) is a rare autosomal recessively… …   Wikipedia

• LDL apheresis — In medicine, LDL apheresis is a form of apheresis, resembling dialysis, to eliminate the cholesterol containing particle low density lipoprotein (LDL) from the bloodstream.UsesIt is used in diseases featuring high LDL, such as the rare homozygous …   Wikipedia

• metabolic disease — ▪ pathology Introduction       any of the diseases or disorders that disrupt normal metabolism, the process of converting food to energy on a cellular (cell) level. Thousands of enzymes participating in numerous interdependent metabolic pathways… …   Universalium

• Carnitine palmitoyltransferase II deficiency — Classification and external resources Carnitine ICD 9 …   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