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Homozygous Familial Hypercholesterolemia

Homozygous Familial Hypercholesterolemia: Introduction

Homozygous Familial Hypercholesterolemia: Homozygous Familial Hypercholesterolemia is a severe inherited condition involving abnormal lipid metabolism. Cholesterol levels tend to be very high with problems occurring early in life. Death from a heart attack can occur within the first few years of life in severe cases. More detailed information about the symptoms, causes, and treatments of Homozygous Familial Hypercholesterolemia is available below.

Symptoms of Homozygous Familial Hypercholesterolemia

Treatments for Homozygous Familial Hypercholesterolemia

  • Dietary and lifestyle changes, plasmapheresis to remove VLDL and LDL from the blood and liver transplant in severe cases. Cholesterol-lowering medication is usually ineffective for this condition
  • more treatments...»

Home Diagnostic Testing

Home medical testing related to Homozygous Familial Hypercholesterolemia:

Wrongly Diagnosed with Homozygous Familial Hypercholesterolemia?

Homozygous Familial Hypercholesterolemia: Complications

Review possible medical complications related to Homozygous Familial Hypercholesterolemia:

Causes of Homozygous Familial Hypercholesterolemia

Read more about causes of Homozygous Familial Hypercholesterolemia.

Homozygous Familial Hypercholesterolemia: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Homozygous Familial Hypercholesterolemia

Metabolic syndrome often undiagnosed: Metabolic syndrome, also known as Syndrome X, is an often overlooked medical condition that causes a cluster of chronic...read more »

Heart attacks can be undiagnosed: Although the most severe symptoms of heart attack are hard to miss, there are varying degrees of severity. It is altogether too common for people to die from undiagnosed...read more »

Heart attacks can be overdiagnosed: Although many people die from heart attacks, there are also many cases where people fear that they have a heart attack,...read more »

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, but often fails to be correctly diagnosed. Women with...read more »

Homozygous Familial Hypercholesterolemia: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Homozygous Familial Hypercholesterolemia

Research quality ratings and patient safety measures for medical facilities in specialties related to Homozygous Familial Hypercholesterolemia:

Choosing the Best Hospital: More general information, not necessarily in relation to Homozygous Familial Hypercholesterolemia, on hospital performance and surgical care quality:

Homozygous Familial Hypercholesterolemia: Rare Types

Rare types of diseases and disorders in related medical categories:

Evidence Based Medicine Research for Homozygous Familial Hypercholesterolemia

Medical research articles related to Homozygous Familial Hypercholesterolemia include:

Click here to find more evidence-based articles on the TRIP Database

Homozygous Familial Hypercholesterolemia: Animations

Prognosis for Homozygous Familial Hypercholesterolemia

Prognosis for Homozygous Familial Hypercholesterolemia: The prognosis can be influenced by the level of adherence to the treatment plan but death usually occurs by the end of early adulthood.

Research about Homozygous Familial Hypercholesterolemia

Visit our research pages for current research about Homozygous Familial Hypercholesterolemia treatments.

Statistics for Homozygous Familial Hypercholesterolemia

Homozygous Familial Hypercholesterolemia: Broader Related Topics

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Related Homozygous Familial Hypercholesterolemia Info

More information about Homozygous Familial Hypercholesterolemia

  1. Homozygous Familial Hypercholesterolemia: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Types
  8. Complications
  9. Prognosis
 

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