Familial partial lipodystrophy, Köbberling type (Q97030)
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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 |
||
| 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. |
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CID11:ID_1790224502
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dki-india-ID_1790224502
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