Hyperlipoproteinemia type I

What is hyperlipoproteinemia type I?

Hyperlipoproteinemia type I is a rare inherited condition caused by lipoprotein lipase (LPL) deficiency that results in the impairment of the breakdown of fat. With LPL deficiency, triglycerides accumulate and may lead to other conditions, e.g. enlarged spleen/liver, pancreatitis, and skin lesions.

How do members experience hyperlipoproteinemia type I?

Top 5 symptoms reported by people with hyperlipoproteinemia type I*

*Reports may be affected by other conditions and/or medication side effects. We ask about general symptoms (anxious mood, depressed mood, fatigue, pain, and stress) regardless of condition.

Are you experiencing one or more of these symptoms? Check your symptoms and clarify your options for care using

Top treatments taken by people for hyperlipoproteinemia type I*

We currently don't have enough shared data that is made public for this condition.

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Who has hyperlipoproteinemia type I on PatientsLikeMe?

Age

Age Proportion # of patients
<20 0
20s 3
30s 1
40s 5
50s 2
60s 5
70+ 6

Distribution of sex

Sex

Sex Proportion # of patients
Male 6
Female 16
Learn more about our community’s experience with hyperlipoproteinemia type I.

Talk to people with hyperlipoproteinemia type I

24

24

members say they have this condition

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Endocrine, Metabolism and Nutrition

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