PPT-7-5 Phenylketonuria Report

By Kevin Zhu Walter Chen and Sachin Patro Definition Phenylketonuria PKU is a genetic disorder that is described by an lack of ability of the body to use the necessary amino acid called phenylalanine Amino acids are the building blocks for bodys proteins Essential amino acids can only be attained from the food that we eat Our body does not normally produce them The classic PKU the enzyme that breaks down phenylalanine hydroxylase is absolutely or almost completely lacking This enzyme normally turns phenylalanine to another amino acid called tyrosine Without this Classic PKU phenylalanine and its other breakdown chemicals from other enzyme method build up in the blood and body tissues . 57347E57347LQFUHDVLQJ57347LQYHVWPHQW57347LQ57347WKH57347UH57567QHPHQW57347 5744157454574445737657458574495744757455574585745557461574595737657445574625744157452574615744157460574495745557454573765745557446573765746057448574455737657453574555745957460 In the world today there are an estimated 130140 million girls and women who have been subjected to the operation and 3 million girls are at risk of undergoing the practice every year 1 Studies indicate that the practice of FGM has changed in a num O Box 2225 Ponte Vedra Beach FL 32004 Phone 9046142001 Email stanstantheannuity mancom brPage 2br VitalSigns Company List Page 2 of 18 Data for YearEnd 2012 from the life insurance companies statutory annual statements This information represents onl O Box 2225 Ponte Vedra Beach FL 32004 Phone 9046142001 Email stanstantheannuity mancom brPage 2br VitalSigns Company List Page 2 of 20 Data for YearEnd 2011 from the life insurance companies statutory annual statements This information represents onl Vol1 No1 2010 unpublished 2007 Fiji Situation Report brPage 10br brPage 11br brPage 12br NHA 2007 2008 brPage 13br 5 year Annual Annual STRATEGIC PLAN CORPORATE PLANS Business Plans Business Plans PERFORMANCE INDICATORS ACHIEVED OR UNACHIEVED brPag 5 of the Food and Agricultural Code The Final Grape Crush Report includes all grape tonnag e crushed during the 2013 season Changes in tonnage Brix and prices from the preliminary report to this final report were due to late repor ts and corrections Tam Nguyen. CHEM 4700. Introduction. PKU is a . common inborn metabolic . disorder caused by a deficiency of the liver enzyme phenylalanine hydroxylase. . It . prevents normal . metabolization. of phenylalanine (. By: Adrienne Gebele. What is PKU?. 1. Inherited disorder. Occurrence varied due to ethnicity and geography. About 1 and 10,000 to 15,000 infants are born with in the U.S.. People born with PKU have an inactive liver enzyme which causes a dangerous build up of phenylalanine in the blood. BY: MELISSA MORALES. PRACTICE BEFORE IMPLEMENTATION. PRIOR TO JANUARY 5, 2015. IN OUR HOSPITAL, IN OUR UNIT EMERGENCY DEPARTMENT, SHIFT REPORT WOULD TAKE PLACE IN THE NURSES STATION BY ONCOMING AND LEAVING SHIFT AT NO POINT DID BOTH NURSES WENT TO PATIENTS ROOM TO VERIFY THE “SHIFT REPORT” WAS ACCURATE AND MUCH LESS WAS THE PATIENT INVOLVED. . Biologia Celular e Molecular II. 2012/2013. Work done by:. Cátia Ferreira (T5). Isa Costa (T6) . Jéssica Vasconcelos (T5). Sara Ferreira (T6). Cellular and Molecular . M. echanisms in Phenylketonuria. Through Modeling. Background Information. Robert Guthrie, M.D., Ph.D.. 1947 son John born disabled. Became interested in the causes and prevention of mental retardation. Son’s disability was never diagnosed. Basic Steps to Schedule Page 1of 7Last Revised 2015-17-04Rightclick on the report Title From the drop down menu click The window is displayed In the left panel click In the panel on the right click t 31313131 CCCHAPTER HAPTER HAPTER 222MMMMOOD OOD OOD DDDISORDERSISORDERSISORDERS Mood disorders include major depression, bipolardisorder (combining episodes of both mania anddepression) and dysthymia. Cary O. Harding, MD. Department of Molecular & Medical Genetics. Disclosures. BioMarin Corporation. Funds for participation in clinical trials. Sapropterin dihydrochloride. rAvPAL-PEG. National PKU Alliance.