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Phenylketonuria PKU An Inborn Error of Metabolism
Author: Anonymous
Institution

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American Academy of Pediatrics: Committee on Genetics. (2001). Maternal Phenylketonuria. .... Journal of Pediatrics. 124:388-92. Tolstoi, L. G. (2000). …www4.cord.edu/fns/portfolios/hmpowers/Phenylketonuria%20(PKU).ppt
Phenylketonuria PKU
Author: Anonymous
Institution

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PKU Genetics . The PKU gene is found on the q arm of chromosome 12, locus 24.1 in the phenylalanine hydroxylase gene
Biology 22 Genetics and Molecular Biology
Author: Anonymous
Institution

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Phenylketonuria (PKU) is a genetic disorder that is characterized by an inability of the body to utilize the essential amino acid, phenylalanine.
PHENYLKETONURIA PKU
Author: Anonymous
Institution

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A strictly controlled phenylalanine free diet ; up to the age of about 14 years old; phenylalanine is itself an essential amino acid small doses must be supplied; After this
Phenylketonuria PKU is an inherited defect in phenylalanine metabolism in
Author: Anonymous
Institution

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Phenylketonuria (PKU) is an inherited defect in phenylalanine metabolism in which phenylalanine hydroxylase is the defective enzyme. This enzyme produces tyrosine from
Phenylketonuria PKU
Author: Anonymous
Institution

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of an educator with a student who has PKU helping to maintain his or her phenylalanine-restricted diet, careful avoidance of the sugar substitute aspartame ("Nutrasweet
Phenylketonuria PKU
Author: Anonymous
Institution

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Must avoid high-protein foods: milk, ice cream, eggs, nuts, beans, chicken, steak and fish. As well as diet sodas and aspartame. The treatment is continued for life
Critical Care Nursing A Holistic Approach Part 2
Author: Anonymous
Institution

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Genetic Disease . Monogenic – A single mutant gene; Sickle cell anemia; Cystic fibrosis; Phenylketonuria ; Cytogenetic – Addition/Deletion of a chromosome
PPT- Phenylketonuria is an inherited disease caused by a recessive . - Slideworld Medical Search Engines
Author: Anonymous
Institution

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PPT- Phenylketonuria is an inherited disease caused by a recessive autosomal allele. If a woman and her husband are both carriers, what is the probability that their first child
Health Problems of Newborns
Author: Anonymous
Institution

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Inborn Errors of Metabolism. Congenital hypothyroidism; Phenylketonuria (PKU); Galactosemia. Mosby items and derived items © 2005, 2001 by Mosby, Inc. ...
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