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
See full list of 6
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...»
Read more about treatments for Homozygous Familial Hypercholesterolemia
Home Diagnostic Testing
Home medical testing related to Homozygous Familial Hypercholesterolemia:
- High Cholesterol: Home Testing:
- High Blood Pressure: Home Testing
- more...»
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...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...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, but actually have something milder.
Some of the conditions which may...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...read more »
Read more about Misdiagnosis and Homozygous Familial Hypercholesterolemia
Homozygous Familial Hypercholesterolemia: Research Doctors & Specialists
Research related physicians and medical specialists:
- Cholesterol Specialists:
- Cardiac (Heart) Specialists:
- Blood Health Specialists (Hematology):
- more specialists...»
Other doctor, physician and specialist research services:
Hospitals & Clinics: Homozygous Familial Hypercholesterolemia
Research quality ratings and patient safety measures
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Choosing the Best Hospital:
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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
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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.
More about prognosis of Homozygous Familial Hypercholesterolemia
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
Types of Homozygous Familial Hypercholesterolemia
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