Examples of 'familial hypercholesterolaemia' in a sentence
Meaning of "familial hypercholesterolaemia"
Refers to an inherited genetic disorder characterized by high levels of cholesterol in the blood. It is caused by mutations in specific genes involved in cholesterol metabolism and transport. Familial hypercholesterolaemia increases the risk of developing cardiovascular diseases, such as heart attacks and strokes, at a young age
How to use "familial hypercholesterolaemia" in a sentence
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familial hypercholesterolaemia
Clinical efficacy in homozygous familial hypercholesterolaemia.
Homozygous familial hypercholesterolaemia as an adjunct to diet and other lipid lowering treatments e . g.
Treatment of homozygous familial hypercholesterolaemia.
No difference in safety was observed between adolescent and adult patients with homozygous familial hypercholesterolaemia.
Heterozygous familial hypercholesterolaemia.
Inclisiran is an experimental drug for the treatment of familial hypercholesterolaemia.
Children and adolescents with heterozygous familial hypercholesterolaemia No pharmacokinetic data in children are available.
Pravastatin has not been evaluated in patients with homozygous familial hypercholesterolaemia.
Homozygous familial hypercholesterolaemia in adults and adolescents aged 12 years and over.
Some people have high cholesterol because of an inherited condition called familial hypercholesterolaemia.
Treatment of homozygous familial hypercholesterolaemia as an adjunct to diet and other lipid lowering treatments e . g.
Statins can also be used to treat people with a condition called familial hypercholesterolaemia.
A total of 102 severe familial hypercholesterolaemia patients and 96 homozygous familial hypercholesterolaemia patients enrolled in TAUSSIG.
The invention is also particularly suitable for prevention or treatment of homozygous familial hypercholesterolaemia.
Anyone, even children, with a family history of familial hypercholesterolaemia should have their cholesterol measured.
See also
Outcome of case finding among relatives of patients with known heterozygous familial hypercholesterolaemia.
Familial hypercholesterolaemia affects about one in 500 people.
Three of the ten studies were conducted exclusively in patients with heterozygous familial hypercholesterolaemia heFH.
Fourteen patients aged ≥ 12 to < 18 years with homozygous familial hypercholesterolaemia were included in clinical studies.
Mutations in the gene encoding the LDL receptor are known to cause familial hypercholesterolaemia.
Long-term efficacy in homozygous familial hypercholesterolaemia.
Treatment of primary hypercholesterolaemia or mixed dyslipidaemia, treatment of homozygous familial hypercholesterolaemia.
A case is presented of a 42 year-old patient with heterozygous familial hypercholesterolaemia treated with PCSK9 inhibitors.
Placebo-controlled phase 3 studies ( on background statin ) in patients with heterozygous familial hypercholesterolaemia heFH.
Anyone, even children, with a family history of familial hypercholesterolaemia.
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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
Examples of using Hypercholesterolaemia
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Primary hypercholesterolaemia and mixed dyslipidaemia in adults
It is used to lower cholesterol in people with hypercholesterolaemia
That diet induces hypercholesterolaemia and hypertriglyceridaemia
