1 Meeting Children’s Special Food and Nutrition Needs in Child Nutrition Programs Lesson 4: Understanding Inborn Errors of Metabolism Define inborn errors.

Slides:



Advertisements
Similar presentations
Alterations in Metabolic Status Jan Bazner-Chandler RN, MSN, CNS, CPNP.
Advertisements

Phenylketonuria (PKU)
Learning Objectives Summarize key components regarding food allergies.
Copyright © 2003 Delmar Learning, a Thomson Learning company Section 2 Maintenance of Health Through Good Nutrition.
Copyright © 2011 Delmar, Cengage Learning. ALL RIGHTS RESERVED. Chapter 12 Diet during Infancy.
1 Focus on the Customer Building a Customer-Focused School Nutrition Program.
Scene 1: Michelle is saved by the starving bacteria
IN THE NAME OF GOD phenylketonuria.
Honey Bee Nutrition And Feeding
PKU Phenylketonuria Polly Bainbridge Samantha Miller Madison Mitchell.
AMINO ACIDS.
Metabolism of disaccharides: Fructose and Galactose Dr. Sooad Al-Daihan Biochemistry department.
INHERİTED DİSEASES OF AMİNO ACİD METABOLİSM Prof.Dr.Arzu SEVEN 1.
Postnatal Screening – Diagnostic testing for metabolic disorders.
CARBOHYDRATE METABOLISM- INHERITED DISORDERS DR. Tagreed Osman.
Agenda:  What is a Special Diet?  What is a Disability?  Allergies vs. Food Intolerances  Disabilities and Special Dietary Needs  Attention-Deficit.
MAPLE SYRUP URINE DISEASE (MSUD) IS A METABOLISM DISORDER PASSED DOWN THROUGH FAMILIES IN WHICH THE BODY CANNOT BREAK DOWN CERTAIN PARTS OF PROTEINS. URINE.
1 Meeting Children’s Special Food and Nutrition Needs in Child Nutrition Programs 2006 Breakfast Lunch Training National Food Service Management Institute.
Carbohydrate Notes.
Genetic Disorders.
Food Purchasing for Child Care National Food Service Management Institute The University of Mississippi
PKU Phenylketonuria. What is PKU? PKU (phenylketonuria), is a rare, inherited metabolic disease that affects the way the body processes protein. People.
Inborn Errors of Metabolism Monica Egan. Video Links Part 1: – xWwY&feature=plcphttp://
 By: Christer Löfkrantz and Nita Helseth.  Autosomal recessive disorder  Protein complex BCKD (Branched- chain alpha-ketoacid dehydrogenase)  Mutations.
Section 3.  Recommended Dietary Allowances (RDAs)- recommended nutrient intakes that will meet the needs of almost all healthy people  Daily value (DV)-
SB1bc Test Review Macromolecules and Enzymes. Since enzymes are proteins they are made of ……what? Amino acids joined by peptide bonds.
1 Meeting Children’s Special Food and Nutrition Needs in Child Nutrition Programs Lesson 4: Understanding Inborn Errors of Metabolism Define inborn errors.
1 Meeting Children’s Special Food and Nutrition Needs in Child Nutrition Programs Lesson 2: Helping Students with Diabetes Define diabetes and explain.
Genetic disorders C.1.m. – Describe the mode of inheritance of commonly inherited disorders.
Food Purchasing for Child Care National Food Service Management Institute The University of Mississippi
1 Food Intolerances and Allergies. 2 How common are food allergies?
Case Study: Phenylketonuria (PKU)
HEREDITARY METABOLIC DISEASES. Particular risk factors are: Advanced maternal age (e.g. Down's syndrome) Family history of inherited diseases (e.g. fragile.
Phenylketoriuria (PKU)
What Do You Know About PKU?
1 Section 5 ________ Child Nutrition Programs 5-1 Other Foods.
Nutrition Maintaining a Healthy Weight Nutrients Dietary Guidelines Misc
National Food Service Management Institute The University of Mississippi The Tools for Guiding Food Choices.
Maple Syrup Urine Disease (MSUD)
1 Infants: Understanding Growth and Development. 2 If you could be a baby again you would…
1 Meeting Children’s Special Food and Nutrition Needs in Child Nutrition Programs Lesson 5: Managing Celiac Disease.
Diet and Nutrition Complete diets Cost Allergies Quality ingredients Weight management Special needs.
Portion Control Visual 1. Visual 2 Introduction The last customer deserves the same quality as the first customer.
1 Cost-Effective Shopping. 2 What is cost-effective shopping?
The Energy Nutrients. National Food Service Management Institute The University of Mississippi 2 Physical Activity Booster Strength.
Nutritional therapy in children with in-born errors of metabolism.
Metabolic Pathways. Metabolic pathway A metabolic pathway is a series of enzyme-controlled chemical reactions that convert compounds from a precursor.
1 This training is conducted by the National Food Service Management Institute The University of Mississippi
ORIENTATION TO SCHOOL NUTRITION MANAGEMENT. Identify major legislation related to disabilities.
Lesson 1 T1 FOOD SERVICE …you are important ASSISTANT YOU MAKE IT HAPPEN!
NEWBORN SCREENING SAVE YOUR BABY from MENTAL RETARDATION ZHALLENE MICHELLE E. SANCHEZ.
Lesson 3 T1 FOOD SERVICE …you are important ASSISTANT WORK AS A TEAM.
Mr. Adham Ahmed Diet During Infancy. Mr. Adham Ahmed2 Objectives  State the effect inadequate nutrition has on an infant  Identify the ingredients used.
Chapter 4: Carbohydrates Plants Synthesize Glucose.
KA 4: Ante- and postnatal screening
Scene 1: Michelle is saved by the starving bacteria
Metabolism in Nervous Tissue
Regulator gene Produces a protein called the repressor molecule
Nutrition Management of Maple Syrup Urine Disease
FOOD SERVICE ASSISTANT …you are important COMMUNICATE FOR SUCCESS.
Accommodating Special Dietary Needs
Meeting Children’s Special Food and Nutrition Needs in Child Nutrition Programs Lesson 2: Helping Students with Diabetes Learning Objectives Define diabetes.
Inborn Error of Metabolism
HEREDITARY METABOLIC DISEASES
Carbohydrates, Fats, and Proteins
Maple syrup urine By:Ulysees Wingo Jr..
Phenylketonuria (PKU) is a rare genetic condition in which a baby cannot “metabolize,” or digest, an essential amino acid called phenylalanine that is.
PHENYLKETONURIA (PKU) BY: BORA LUCAJ.
Maple Syrup Urine By: Joe Harvey.
Lesson 3 Terms and Definitions
Presentation transcript:

1 Meeting Children’s Special Food and Nutrition Needs in Child Nutrition Programs Lesson 4: Understanding Inborn Errors of Metabolism Define inborn errors of metabolism, identify the more common errors, and explain dietary treatment for children with inborn errors of metabolism. Describe cafeteria accommodations for these children and understand the need for a professional consultant in difficult cases. Learning Objectives

2 Inborn Errors of Metabolism Rare genetic disorders in which the body cannot metabolize food normally By-products of metabolism, amino acids, sugars, fatty acids build up in the body, causing serious complications Dietary treatment: strict diet management to avoid toxic buildup of dietary by-products Special foods or formulas may be needed

3 Phenylketonuria (PKU) Cannot process the amino acid phenylalanine Dietary treatment: –low-protein diet (to prevent increase in phenylalanine) –special formula to provide protein

4 Galactosemia Cannot process the sugar galactose Dietary treatment: no milk or dairy products

5 Hereditary Fructose Intolerance Cannot process the sugar fructose Dietary treatment: –no fructose (high-fructose corn syrup, honey, fruit) –no sucrose (table sugar)

6 Maple Syrup Urine Disease Cannot process the branched chain amino acids leucine, isoleucine, valine Dietary treatment: –low-protein diet –special formula to provide protein

7 Food Service Assistants Maintain communication among parents, teacher, school nurse, food service, and consultant if needed Understand the dietary restrictions prescribed in the plan kept on file with the school nurse Obtain and serve special formula or foods Follow prescribed portion sizes Report mistakes immediately Keep information confidential

8 This training was conducted by the National Food Service Management Institute The University of Mississippi

9 National Food Service Management Institute The University of Mississippi Mission: To provide information and services that promote the continuous improvement of child nutrition programs Vision: To be the leader in providing education, research, and resources to promote excellence in child nutrition programs