Hyperlipidaemia type 3 - familial defective apolipoprotein B (Q102527): Difference between revisions

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Envolve níveis anormalmente elevados de qualquer ou todos os lipídios e/ou lipoproteínas séricas. Esta forma é devido a quilomícrons elevados e IDL (lipoproteína de densidade intermediária). Também conhecida como doença beta ampla ou disbetalipoproteinemia, a causa mais comum dessa forma é a presença do genótipo ApoE E2/E2. É devida a colesterol rico em VLDL. Este diagnóstico é devido a um defeito na apolipoproteína B, e é familiar.
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This involves abnormally elevated levels of any or all lipids and/or lipoproteins in the blood. This form is due to high chylomicrons and IDL (intermediate density lipoprotein). Also known as broad beta disease or dysbetalipoproteinaemia, the most common cause for this form is the presence of ApoE E2/E2 genotype. It is due to cholesterol-rich VLDL. This diagnosis is with familial defective apolipoprotein B.

Revision as of 19:34, 16 August 2026

This involves abnormally elevated levels of any or all lipids and/or lipoproteins in the blood. This form is due to high chylomicrons and IDL (intermediate density lipoprotein). Also known as broad beta disease or dysbetalipoproteinaemia, the most common cause for this form is the presence of ApoE E2/E2 genotype. It is due to cholesterol-rich VLDL. This diagnosis is with familial defective apolipoprotein B.
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    Hyperlipidaemia type 3 - familial defective apolipoprotein B
    This involves abnormally elevated levels of any or all lipids and/or lipoproteins in the blood. This form is due to high chylomicrons and IDL (intermediate density lipoprotein). Also known as broad beta disease or dysbetalipoproteinaemia, the most common cause for this form is the presence of ApoE E2/E2 genotype. It is due to cholesterol-rich VLDL. This diagnosis is with familial defective apolipoprotein B.

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