'Phenylketonuria pku' diaporamas de présentation

Amino Acids Dietary proteins are the primary source of a.a.s for endogenous protein synthesis.

Amino Acids Dietary proteins are the primary source of a.a.s for endogenous protein synthesis.

1.37k views • 99 slides

Amino acid disorders

Amino acid disorders. Phenylketonuria (PKU). Enzyme defect : phenylalanine hydroxylase (12th chromosome): more than 400 mutations I ncidence : Average 1:10,000 (Highest incidence in Turkey, 1: 4,0 00). Phenylketonuria (PKU) : Variants.

799 views • 57 slides

Mutation, DNA repair, and Evolution (with references to disease, including aging and cancer)

Mutation, DNA repair, and Evolution (with references to disease, including aging and cancer). Objectives :. 1. Define the nature of genetic variation. 2. Provide a context for understanding mutation (disease and aging).

677 views • 55 slides

Phenylketonuria (PKU) screening

Phenylketonuria (PKU) screening. Pre-activity assessment questions. Note: The first two slides are intended for first-time clicker users to become accustomed to the devices. Where do you live?. Baltimore area Washington area Salisbury Other than Salisbury on the Eastern Shore of MD

1.02k views • 44 slides

Phenylketonuria (PKU) screening

Phenylketonuria (PKU) screening. Pre-activity assessment questions. Note: The first two slides are intended for first-time clicker users to become accustomed to the devices. Where do you live?. Baltimore area Washington area Salisbury Other than Salisbury on the Eastern Shore of MD

892 views • 44 slides

CHEMISTRY AND LIFE

407 views • 21 slides

Phenylketonuria

Phenylketonuria. Connecticut. By: Christie Iorfino and Bianca LeBlanc Period 6. Testing Recommendation. We recommend testing for Phenylketonuria at birth.

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Phenylketonuria in Connecticut

Phenylketonuria in Connecticut. Derek Krewson Gunnar Cedergren Berechid Class 4. Testing Recommendations. Phenylketonuria (PKU) is a highly recommended genetic test by healthcare professionals, the United States Preventative Services Task Force (USPSTF) and pediatric doctors for newborns.

290 views • 11 slides

Phenylketonuria (PKU)

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PKU - Phenylketonuria

Mama Mia Sofia [Thai] Damonster [a.k.a. Damani J.]. PKU - Phenylketonuria. What is it?. Phenylketonuria (PKU) is a rare condition in which a baby is born without the ability to properly break down an amino acid called phenylalanine. What are the symptoms?.

227 views • 10 slides

Phenylketonuria (PKU)

Phenylketonuria (PKU). By: Lynn Reynolds. How is PKU Inherited?. PKU is an autosomal recessive trait Both parents must be carriers of the trait for the child to show symptoms If both parents are carriers, the child has a 25% chance of having the disease.

195 views • 10 slides

Phenylketonuria (PKU)

Phenylketonuria (PKU). By Carter Rolfe. What is Phenylketonuria?. Phenylketonuria, or PKU for short, is a genetic disorder found in infants.

778 views • 9 slides

Phenylketonuria Treatment Market - Global Industry Insights, Trends, Outlook

Phenylketonuria (PKU) is a rare genetic disorder caused due to increased level of phenylalanine in the blood.

89 views • 8 slides

Phenylketonuria (PKU) Products Under Development, H2 2015

Phenylketonuria (PKU) - Pipeline Review, H2 2015 report provides an overview of the Phenylketonuria (PKU)'s therapeutic pipeline.

287 views • 7 slides