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 belowLipoprotein Lipase Deficiency (LPLD) Resources
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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.