Analphalipoproteinaemia (Q97098): Difference between revisions
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A doença de Tangier é uma hipoalfalipopproteinemia hereditária recessiva, caracterizada por deposição de colesterol na córnea, amígdalas, reto, fígado e baço, e algumas vezes associada a sintomas neurológicos. | |||
| description / en | description / en | ||
Tangier disease is a recessively inherited hypoalphalipopproteinaemia characterised by cholesterol deposition in the cornea, tonsils, rectum, liver and spleen, and sometimes associated with neurologic symptoms. | |||
Revision as of 13:08, 16 August 2026
Tangier disease is a recessively inherited hypoalphalipopproteinaemia characterised by cholesterol deposition in the cornea, tonsils, rectum, liver and spleen, and sometimes associated with neurologic symptoms.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1796662502 |
||
| English | Analphalipoproteinaemia |
Tangier disease is a recessively inherited hypoalphalipopproteinaemia characterised by cholesterol deposition in the cornea, tonsils, rectum, liver and spleen, and sometimes associated with neurologic symptoms. |
