Examples of 'familial hypercholesterolemia' in a sentence
Meaning of "familial hypercholesterolemia"
familial hypercholesterolemia: An inherited genetic disorder characterized by high levels of cholesterol, specifically low-density lipoprotein (LDL) cholesterol, leading to an increased risk of heart disease and other related health complications
How to use "familial hypercholesterolemia" in a sentence
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familial hypercholesterolemia
Familial hypercholesterolemia is a form of inherited high cholesterol.
That facilitates a definitive diagnosis of familial hypercholesterolemia.
Familial hypercholesterolemia twice as common as previously believed.
The true prevalence of familial hypercholesterolemia remains unknown.
Familial hypercholesterolemia is inherited in families in an autosomal dominant manner.
They are often a symptom of familial hypercholesterolemia.
Homozygous familial hypercholesterolemia and its management.
I am the one who diagnosed the familial hypercholesterolemia.
Familial hypercholesterolemia is the name given to such a condition.
Read more about familial hypercholesterolemia.
It is further disclosed that the medicament is for treating familial hypercholesterolemia.
How common is familial hypercholesterolemia.
Lipoprotein apheresis is a procedure that can be used to treat familial hypercholesterolemia.
Few adults who experience familial hypercholesterolemia die prematurely.
In children statins are effective at reducing cholesterol levels in those with familial hypercholesterolemia.
See also
Living with familial hypercholesterolemia.
This is one of the main differential diagnoses in patients with suspected familial hypercholesterolemia.
Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics.
It is used only in patients who have familial hypercholesterolemia.
Also individuals having familial hypercholesterolemia can be treated with agents identified herein.
Reduction of serum cholesterol in two patients with homozygous familial hypercholesterolemia by dichloroacetate.
Familial hypercholesterolemia is a genetic disorder in which very high cholesterol levels run in families.
Genetic abnormalities such as familial hypercholesterolemia.
Familial hypercholesterolemia is a condition that affects the manner in which your body processes cholesterol.
Genetic screening is now advised if a form of familial hypercholesterolemia is suspected.
Familial hypercholesterolemia This is felt to be irritation secondary to tendon xanthomatosis a cholesterol deposit.
The gene mutation that causes familial hypercholesterolemia is passed from parent to child.
There are three different known mutations that can lead to a diagnosis of familial hypercholesterolemia.
People with the inherited condition familial hypercholesterolemia have very high LDL levels.
Three of the five studies were conducted exclusively in patients with heterozygous familial hypercholesterolemia HeFH.
Also associated with familial hypercholesterolemia FH.
Kynamro was also approved in the United States for the treatment of homozygous familial hypercholesterolemia.
Having Familial Hypercholesterolemia means you have very high cholesterol from birth.
Mutations in the LDL receptor gene cause familial hypercholesterolemia.
Unfortunately, most cases of familial hypercholesterolemia remain undiagnosed and undertreated, he said.
Xanthomas on the Achilles tendon are specific to Familial Hypercholesterolemia.
Possible signs of familial hypercholesterolemia include,.
A de novo mutation of the LDL-receptor gene as the cause of familial hypercholesterolemia.
Expression of the familial hypercholesterolemia gene in heterozygotes, mechanism for a dominant disorder in man ".
The relationship of molecular genetic to clinical diagnosis of familial hypercholesterolemia in a Danish population.
Familial hypercholesterolemia is detected through a blood test, which is carried out on all athletes.
Required Medical Information Diagnosis of homozygous familial hypercholesterolemia as evidenced by one of the following.
According to another preferred embodiment, the disease condition is primary hypercholesterolemia or familial hypercholesterolemia.
Adolescents with a family history of CVD and familial hypercholesterolemia have lower FMD than healthy populations.
Statin treatment is an effective lipid-lowering therapy in children with familial hypercholesterolemia.
Familial hypercholesterolemia is an autosomal-dominant disorder that often causes premature coronary artery disease.
Recommendations for treatment of familial hypercholesterolemia include,.
There is a clear need for alternative treatments for those patients exhibiting hypercholesterolemia, particularly familial hypercholesterolemia.
Homozygous and heterozygous familial hypercholesterolemia ( hoFH, heFH ) is a condition associated with premature atherosclerotic vascular disease.
Inherited metabolic disorders, such as familial hypercholesterolemia.
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Examples of using Hypercholesterolemia
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Familial hypercholesterolemia is a form of inherited high cholesterol
Statins are widely used in the treatment of hypercholesterolemia
Familial hypercholesterolemia twice as common as previously believed
Examples of using Familial
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Familial demands on women contribute to gender inequality
I have kicked a few familial hornets nests
Both familial and sporadic forms occur
