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Aortic Coarctation : Risk Factors

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Bicuspid aortic valve is the most common malformation of the heart valves. In this type of deformity, the aortic valve has only two cusps, which are rigid points such as that seen on leaves, instead of the three cusps normally present.
Source:Gale Encyclopedia of Genetic Disorders Part II
A bicuspid aortic valve is an aortic valve that only has two leaflets, instead of three.The aortic valve regulates blood flow from the heart into the aorta, the major blood vessel that brings blood to the body.The aortic valve allows oxygen-rich b...
Source:ADAM
Date:April 30, 2008
Bicuspid aortic valve is the most common malformation of the heart valves. In this type of deformity, the aortic valve has only two cusps, which are rigid points.such as that seen on leaves, instead of the three cusps normally present.
Source:Gale Encyclopedia of Genetic Disorders Part I
Turner syndrome is a chromosomal disorder affecting females wherein one of the two X chromosomes is defective or completely absent.Chromosomes are structures in the nucleus of every cell in the human body. Chromosomes contain the genetic informati...
Source:Gale Encyclopedia of Genetic Disorders Part II
Turner syndrome is a genetic condition in which a female does not have the usual pair of two X chromosomes.Bonnevie-Ullrich syndrome; Gonadal dysgenesis; Monosomy X.Humans have 46 chromosomes. Chromosomes contain all of your genes and DNA, the bui...
Source:ADAM
Date:September 26, 2007
Detailed information on Turner syndrome, including causes, diagnosis, and prevention
Source:StayWell
Detailed information on Turner syndrome, including causes, diagnosis, and prevention
Source:StayWell
Turner syndrome is a chromosomal disorder affecting females wherein one of the two X-chromosomes is defective or completely absent.Chromosomes are structures in the nucleus of every cell in the human body. Chromosomes contain the genetic informati...
Source:Gale Encyclopedia of Genetic Disorders Part I
Turner syndrome is a chromosomal disorder affecting females wherein one of the two X-chromosomes is defective or completely absent.Chromosomes are structures in the nucleus of every cell in the human body. Chromosomes contain the genetic informati...
Source:Gale Encyclopedia of Medicine
The underlying chromosomal defect was discovered in 1959. Turner syndrome occurs in approximately one out of every 2,500 live births.
Source:Gale Encyclopedia of Childhood and Adolescence
What treatments should be considered when you have been diagnosed with Turner's syndrome?
Source:StayWell
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