Hyperlipoproteinaemia type 1 (Q98421): Difference between revisions
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A hiperlipoproteinemia tipo I existe em várias formas: Deficiência de lipoproteína lipase (Tipo Ia), devido a uma deficiência de lipoproteína lipase ou apolipoproteína C2 alterada, resultando em aumento de quilomícrons, as partículas que transferem ácidos graxos do trato digestivo para o fígado. Deficiência familiar de apoproteína CII (Tipo Ib), uma condição causada pela falta de ativador da lipoproteína lipase . Quilomicronemia devido ao inibidor circulante da lipoproteína lipase(Tipo Ic). A hiperlipoproteinemia do tipo I geralmente se apresenta na infância com xantoma eruptivo e cólica abdominal. As complicações incluem oclusão da veia retiniana, pancreatite aguda, esteatose, organomegalia e lipemia retinal. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Type I hyperlipoproteinemia exists in several forms: Lipoprotein lipase deficiency (Type Ia), due to a deficiency of lipoprotein lipase (LPL) or altered apolipoprotein C2, resulting in elevated chylomicrons, the particles that transfer fatty acids from the digestive tract to the liver. Familial apoprotein CII deficiency (Type Ib), a condition caused by a lack of lipoprotein lipase activator. Chylomicronemia due to circulating inhibitor of lipoprotein lipase (Type Ic). Type I hyperlipoproteinemia usually presents in childhood with eruptive xanthomata and abdominal colic. Complications include retinal vein occlusion, acute pancreatitis, steatosis and organomegaly, and lipaemia retinalis. | |||||||||||||||
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CID11:ID_2104488268 | |||||||||||||||
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dki-india-ID_2104488268 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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Latest revision as of 14:52, 16 August 2026
Type I hyperlipoproteinemia exists in several forms: Lipoprotein lipase deficiency (Type Ia), due to a deficiency of lipoprotein lipase (LPL) or altered apolipoprotein C2, resulting in elevated chylomicrons, the particles that transfer fatty acids from the digestive tract to the liver. Familial apoprotein CII deficiency (Type Ib), a condition caused by a lack of lipoprotein lipase activator. Chylomicronemia due to circulating inhibitor of lipoprotein lipase (Type Ic). Type I hyperlipoproteinemia usually presents in childhood with eruptive xanthomata and abdominal colic. Complications include retinal vein occlusion, acute pancreatitis, steatosis and organomegaly, and lipaemia retinalis.
| Language | Label | Description | Also known as |
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| default for all languages | ID_2104488268 |
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| English | Hyperlipoproteinaemia type 1 |
Type I hyperlipoproteinemia exists in several forms: Lipoprotein lipase deficiency (Type Ia), due to a deficiency of lipoprotein lipase (LPL) or altered apolipoprotein C2, resulting in elevated chylomicrons, the particles that transfer fatty acids from the digestive tract to the liver. Familial apoprotein CII deficiency (Type Ib), a condition caused by a lack of lipoprotein lipase activator. Chylomicronemia due to circulating inhibitor of lipoprotein lipase (Type Ic). Type I hyperlipoproteinemia usually presents in childhood with eruptive xanthomata and abdominal colic. Complications include retinal vein occlusion, acute pancreatitis, steatosis and organomegaly, and lipaemia retinalis. |
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CID11:ID_2104488268
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dki-india-ID_2104488268
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Concluído
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15 August 2026
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