Print friendly version
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.
impaired absorption of foods from the digestive tract. Associated genetic disorders includes abetalipoproteinemia, hypobetalipoproteinemia, and chylomicron retention disease. Symptoms of the genetic or familial form of hypolipoproteinemia varies. In hypobetalipoproteinemia the low density lipoprotein (LDL) cholesterol levels are very low, yet people with this syndrome typically have no symptoms nor require treatment. Other forms result in absent or near absent LDL levels and can cause serious symptoms in infancy and early childhood.Hypolipoproteinemia refers to unusually low levels of fats (lipids) in the blood. Low lipid levels may be caused by rare genetic conditions, or be a sign of another disorder such as overactive thyroid, anemia, undernutrition, cancer, chronic infection, or
Last updated: 8/28/2009
- Hypolipoproteinemia . MERCK Manuals. 2008; http://www.merck.com/mmhe/sec12/ch157/ch157c.html. Accessed 8/28/2009.
- The Merck Manuals Online Medical Library provides information on this condition. Click on the link to view the information.
In Depth Information
- MeSH® (Medical Subject Headings) is a terminology tool used by the National Library of Medicine. Click on the link to view information on this topic.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Hypolipoproteinemia. Click on the link to view a sample search on this topic.