Brain Aneurysm : Risk Factors
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Coarctation of the aorta (COA) is a congenital heart defect that develops in the fetus. It involves a constricture of the aorta, the main artery that delivers blood from the left ventricle of the heart to the rest of the body.
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Aortic coarctation is a birth defect in which the major artery from the heart (the aorta) is narrowed somewhere along its length, most commonly just past the point where the aorta and the subclavian artery meet.
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A defect that develops in the fetus in which there is a narrowing of the aortic arch, the main blood artery that delivers blood from the left ventricle of the heart to the rest of the body. Coarctation of the aorta is diagnosed in both newborns and adults.
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Detailed information on coarctation of the aorta, including causes, symptoms, diagnosis, and treatment
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Detailed information on heart defects that cause obstructions in blood flow
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Birth defects are physical abnormalities that are present at birth; they are also called congenital abnormalities. More than 3,000 have been identified.
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Detailed information on birth defects, including their cause and prevention
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Any unusual variation or abnormality in the shape, structure, and/or function of an organ, body part, or tissue is commonly referred to as a birth defect. However, congenital anomaly is the more accurate and preferred term, since birth defect can be misinterpreted to mean a defect produced by the birthing process.
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Women who had a baby with a neural tube defect will need a higher dose of folic acid during this period...
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Detailed information on the identification, treatment, and prevention of birth defects
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Detailed information on evaluating a child for birth defects
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Detailed information on testing for birth defects
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Detailed information on birth defects, including their cause and frequency
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Defects present at birth, resulting from hereditary factors, environmental influences, or maternal illness. Birth or congenital defects are present at birth and result from hereditary factors, environmental influences, or maternal illness.
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What Do You Know About Birth Defects?According to the National Institute of Child Health and Human Development, birth defects are structural or functional abnormalities present at birth that cause physical or mental disability.
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Detailed information on newborn screening for birth defects
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Detailed information on birth defects, including their cause and frequency
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Detailed information on birth defects, including their cause and frequency
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A congenital anomaly may be viewed as a physical, metabolic, or anatomic deviation from the normal pattern of development that is apparent at birth or detected during the first year of life. Under this definition, Mendelian genetic disorders (e.
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Detailed information on birth defects, including their cause and frequency
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Detailed information on the most common types of newborn complications
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Detailed information on cerebral aneurysms, including description of cerebral aneurysms, causes, symptoms, diagnosis, treatment, and full-color anatomical and procedure illustrations
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Polycystic kidney disease (PKD) is one of the most common of all life-threatening human genetic disorders. It is an incurable genetic disorder characterized by the formation of fluid-filled cysts in the kidneys of affected individuals.
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Polycystic kidney disease is an inherited kidney disorder that enlarges the kidneys and interferes with their function because of multiple cysts on the kidneys.
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Detailed information on the different types of polycystic kidney disease, including autosomal dominant polycystic kidney disease, autosomal recessive polycystic kidney disease, and acquired cystic kidney disease
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Two years ago I had a large complex cyst removed from my right kidney. From my symptoms, it seems it has returned. Is this common?
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Polycystic kidney disease (PKD) is one of the most common of all life-threatening human genetic disorders . It is an incurable genetic disorder characterized by the formation of fluid-filled cysts in the kidneys of affected individuals.
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Polycystic kidney disease (PKD) is one of the most common of all life-threatening human genetic disorders . It is an incurable genetic disorder characterized by the formation of fluid-filled cysts in the kidneys of affected individuals.
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