Welcome - Lipoprotein Lipase Deficiency (LPLD) Community

What is Lipoprotein Lipase Deficiency (LPLD) ?

Lipoprotein Lipase Deficiency, is also known as Type I hyperlipoproteinemia or Familial chylomicronemia. People with LPLD have very high triglyceride levels because they lack lipase, the enzyme that clears fat from the blood. Symptoms include recurrent abdominal pain, fat-filled spots known as ‘eruptive xanthomata’, and attacks of acute pancreatitis.

Source: Participating patient organizations visible below

Lipoprotein Lipase Deficiency (LPLD) Resources

More members stories

Latest Member Stories

Been 15 Years since Diagnosed

by erica3172 published about 1 month ago

I am new on Rareconnect, so Hi! I was diagnosed with LPLD since the age of 1 and now im 15. It has been 15 years since i was diagnosed. My mom has ...

Diagnosis at 8 months

by cynthiaturquot published 5 months ago

I have been living in Quebec for 40 years with familial hyperchylomicronemia syndrome (SHF) or hypertriglyceridaemia type 1. I was born in Quebec, ...

Partners and Patient Groups

RareConnect is a patient-led initiative. Patient organisations partner with EURORDIS, itself an international patient organisation, to create communities and provide moderators from within their network. The following patient groups are official partners of this community.