Hyperlipidaemia type 3 - Apolipoprotein E deficiency (Q102532): Difference between revisions

@@ description / pt-br / description / pt-br @@
+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 devido ao colesterol rico em VLDL. Este diagnóstico é devido à deficiência de apolipoproteína E.
@@ 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 apolipoprotein E deficiency.
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+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-15T00:00:00Z
-Timezone
++00:00
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+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 19:35, 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 apolipoprotein E deficiency.

Language	Label	Description	Also known as
default for all languages	ID_1210107763
English	Hyperlipidaemia type 3 - Apolipoprotein E deficiency	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 apolipoprotein E deficiency.