Hyperlipidaemia type 3 - familial dysbetalipoproteinaemia (Q102529): Difference between revisions
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Isso envolve níveis anormalmente elevados de qualquer ou todos os lipídios e/ou lipoproteínas séricos. 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 ao colesterol rico em VLDL. Este diagnóstico é o de disbetalipoproteinemia familiar | |||
| description / en | description / en | ||
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 dysbetalipoproteinaemia. | |||
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 dysbetalipoproteinaemia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1345883140 |
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| English | Hyperlipidaemia type 3 - familial dysbetalipoproteinaemia |
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 dysbetalipoproteinaemia. |
