How To Use Ketonuria In A Sentence
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Stem cell technology may produce cures for Alzheimer's disease; vascular growth factors may enable the body to produce its own cardiac bypasses; and the elimination of metabolic derangements may cure phenylketonuria and diabetes.
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(Unless you have a genetic disease called phenylketonuria (PKU), which prevents you from digesting the amino acid phenylalanine.
Dr. Joseph Mercola: The Deadly Neurotoxin Nearly EVERYONE Uses Daily (VIDEO)
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Tuberous sclerosis, untreated phenylketonuria and fragile X syndrome are genetic syndromes associated with autism.
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Objective To establish a method with high efficiency in detecting phenylalanine hydroxylase(PAH) gene mutations and hence to rapidly diagnose prenatal fetals with phenylketonuria .
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It would be another quarter of a century before scientists finally identified Carol’s condition she was suffering from phenylketonuria, or PKU, brain degeneration caused by inability in the newborn child to process a chemical called phenyl, a deficiency that can be treated only if detected in its early stages.
PEARL BUCK IN CHINA
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Later it was shown, in collaboration with Collip, that other symptoms of diabetes, namely the ketonuria and the absence of glycogen from the liver, were favourably influenced by the extracts and, with Hepburn, that the respiratory quotient became raised.
John Macleod - Nobel Lecture
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College Dublin, who led the study, hopes that the findings will contribute to the understanding of genetic diversity in the human population and help to identify genetic susceptibility to diseases common in the Irish population such as cystic fibrosis, haemochromatosis and phenylketonuria.
NASIOC
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These conditions include sickle cell anemia, beta thalassemia, phenylketonuria PKU, hypothyroidism,8 and galactosemia.
Pregnancy, Childbirth, and the Newborn
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genetic screening of infants for phenylketonuria
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In the dog the blood sugar rises from normal to 150 to 300 mg per cent; there is glycosuria; ketonemia and ketonuria increase; and there is polyuria and polydipsia.
Bernardo Houssay - Nobel Lecture
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In other words, children with phenylketonuria can and should have a normal productive life.
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Baseline assessments of height, weight, blood pressure, urinary specific gravity, and ketonuria were obtained.
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In the dog the blood sugar rises from normal to 150 to 300 mg per cent; there is glycosuria; ketonemia and ketonuria increase; and there is polyuria and polydipsia.
Bernardo Houssay - Nobel Lecture
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Virtually the only people who cannot consume the artificial sweetener aspartame are those who have a rare hereditary disease called phenylketonuria PKU—and every product that contains aspartame carries a PKU warning on the label.
The Small Change Diet
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Glucose toxicity, which is exhibited as a fasting plasma glucose level greater than 250 mg per dL, and ketonuria, weight loss, or symptomatic hyperglycemia, can be addressed promptly with insulin therapy.
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As an example of the power of environmental effects, consider infants with the genetic disorder PKU (phenylketonuria).
The Volokh Conspiracy » Some Scientists’ Openness to the Possibility of Genetic Differences in Mental Traits Among Racial and Ethnic Groups
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Several diseases are directly caused due to single nucleotide changes such as thalassaemia, muscular dystrophy, phenylketonuria, long QT syndrome, familial hypertrophic cardiomyopathy etc.
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The discovery led to the most effective treatment for the disease (now called phenylketonuria )—a diet low in phenylalanine, which the body converts to phenylpyruvic acid.
DIY DNA: One Father's Attempt to Hack His Daughter's Genetic Code
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Lactic acidosis should be suspected in any diabetic patient with metabolic acidosis lacking evidence of ketoacidosis (ketonuria and ketonemia).
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Persons with a rare hereditary disease known as phenylketonuria must control their phenylalanine intake from all sources, including Aspartame.
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Despite giving himself an increased dose he soon developed hyperglycaemia and ketonuria.
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Years ago all babies were screened for a very rare condition called phenylketonuria PKU with a blood test.
The Official Lamaze® Guide
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For example, read: “Intellectual performance of 36 phenylketonuria patients and their nonaffected siblings” by Dobson, Kushida and Williams (1976) in Pediatrics volume 58, pages53 – 58.
The Volokh Conspiracy » Some Scientists’ Openness to the Possibility of Genetic Differences in Mental Traits Among Racial and Ethnic Groups
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In terms of biochemical genetics, the consequences of a metabolic block may be rectified by dietary limitation of the precursor of an injurious accumulation product, aromatic amino acids in phenylketonuria; or by supplying the essential end product from without the cell, the specific blood protein in hemophilia, or a specific essential nutrient molecule such as a vitamin.
Edward Tatum - Nobel Lecture
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This is generally indicated if the patient is clearly unwell, if she has ketonuria, or if her blood glucose concentration is > 20 mmol/l.
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Organic acidopathies (propionic acidemia, methylmalonic acidemia, biotinidase deficiency, phenylketonuria (PKU) and other disorders)
Biochemical Genetics-Metabolic Disease
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She had normal thyroid function, ketonuria, and mild diffuse ST-T wave changes.
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A classic example of an autosomal recessive inborn error of metabolism is phenylketonuria.
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Objective To establish a simple, accurate and rapid method for screening of the mutant genes in phenylketonuria.
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Samples obtained through screening programme for phenylketonuria and congenital hypothyroidism.
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Newborn screening was pioneered in the 1940s by Robert Guthrie, who, having developed a simple blood test for a form of mental retardation called phenylketonuria PKU, proposed the newborn heel stick test to test for PKU and other “inborn errors of metabolism.”
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