An autosomal recessively inherited disorder caused by mutation of ATP-BINDING CASSETTE TRANSPORTERS involved in cellular cholesterol removal (reverse-cholesterol transport). It is characterized by near absence of ALPHA-LIPOPROTEINS (high-density lipoproteins) in blood. The massive tissue deposition of cholesterol esters results in HEPATOMEGALY; SPLENOMEGALY; RETINITIS PIGMENTOSA; large orange tonsils; and often sensory POLYNEUROPATHY. The disorder was first found among inhabitants of Tangier Island in the Chesapeake Bay, MD.
Pozri aj (FX) v slov.
lipoproteíny, HDL retinitis pigmentosa
Pozri aj (FX) v angl.
Lipoproteins, HDL Retinitis Pigmentosa
Odkazy
(3) - heslo MeSH
predmetové heslo
Počet záznamov: 1
openseadragon
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