Hyperlipoproteinemia Type I

Overview

An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove CHYLOMICRONS and TRIGLYCERIDES from the blood which has a creamy top layer after standing.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Hyperlipoproteinemia Type I

Topic type

Condition

Category

General Healthcare

MeSH classification

C16.320.565.398.465|C18.452.584.500.500.644.237|C18.452.584.563.465|C18.452.648.398.465

Preparing for an appointment about Hyperlipoproteinemia Type I

If you are speaking with a healthcare professional about Hyperlipoproteinemia Type I, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

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