Hyperlipoproteinemia type 1 in Missouri

1 specialist · 1 treatment center for Hyperlipoproteinemia type 1 in Missouri, verified against ClinicalTrials.gov, PubMed, and the NPPES NPI registry.

Hyperlipoproteinemia type 1, also known as familial lipoprotein lipase (LPL) deficiency, familial hyperchylomicronemia, or familial chylomicronemia syndrome (FCS), is a rare inherited disorder of lipid metabolism characterized by a severe elevation of triglycerides and chylomicrons in the blood. The condition is caused…

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Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.

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Specialists in Missouri

Ginger Nicol, MD, MD
Rare Disease / Clinical Research
Washington University School of Medicine
SAINT LOUIS, MO
PI×1

Treatment centers in Missouri

St. Louis Children's Hospital Genetics ↗
St. Louis Children's Hospital / Washington University
St. Louis, MO

Hyperlipoproteinemia type 1 in Missouri

Specialists in Missouri

Treatment centers in Missouri

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