Familial partial lipodystrophy, Köbberling type (Q97030): Difference between revisions
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A lipodistrofia parcial familiar tipo Köbberling pertence ao grupo das síndromes de lipodistrofias caracterizadas por anomalias da distribuição do tecido adiposo e frequentemente associadas a resistência à insulina grave manifesta por hiperinsulinemia (níveis de insulina acima de 20mUI/L), intolerância a carboidratos ou diabetes, hipertrigliceridemia com níveis baixos de lipoproteínas de alta densidade (HDL) e hipertensão arterial. Acantose nigricans, esteatose hepática e síndrome dos ovários policísticos também são frequentes. | |||
| description / en | description / en | ||
Familial partial lipodystrophy, Köbberling type belongs to the group of lipodystrophy syndromes characterised by anomalies of adipose tissue distribution and often associated with severe insulin resistance manifested by hyperinsulinaemia (insulin levels above 20mUI/l), carbohydrate intolerance or diabetes, hypertriglyceridaemia with low levels of high-density lipoproteins (HDL) and arterial hypertension. Acanthosis nigricans, hepatic steatosis and polycystic ovary syndrome are also frequent. | |||
Revision as of 13:03, 16 August 2026
Familial partial lipodystrophy, Köbberling type belongs to the group of lipodystrophy syndromes characterised by anomalies of adipose tissue distribution and often associated with severe insulin resistance manifested by hyperinsulinaemia (insulin levels above 20mUI/l), carbohydrate intolerance or diabetes, hypertriglyceridaemia with low levels of high-density lipoproteins (HDL) and arterial hypertension. Acanthosis nigricans, hepatic steatosis and polycystic ovary syndrome are also frequent.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1790224502 |
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| English | Familial partial lipodystrophy, Köbberling type |
Familial partial lipodystrophy, Köbberling type belongs to the group of lipodystrophy syndromes characterised by anomalies of adipose tissue distribution and often associated with severe insulin resistance manifested by hyperinsulinaemia (insulin levels above 20mUI/l), carbohydrate intolerance or diabetes, hypertriglyceridaemia with low levels of high-density lipoproteins (HDL) and arterial hypertension. Acanthosis nigricans, hepatic steatosis and polycystic ovary syndrome are also frequent. |
