Diagnostic testing is genetic testing to diagnose a childhood condition or conditions that can be treated medically during childhood. An example is retinoblastoma.

Slides:



Advertisements
Similar presentations
Choices in Genetics: The Parent Perspective on Genetics Testing in EHDI Systems National EHDI Conference March 27 th, 2007 Salt Lake City, UT Molly Martzke,
Advertisements

PERSONALIZED MEDICINE: Planning for the Future You, Your Biomarkers and Your Rights.
Areas of Research Specific issues. Clinical Trials Phase I First use in humans of an experimental drug or treatment In a small group of healthy volunteers.
© 2009 NHS National Genetics Education and Development CentreGenetics and Genomics for Healthcare This PowerPoint file contains.
GET THE FACTS ABOUT SCOLIOSIS I.M. Doctor, M.D. My Office My City, State.
Harrison et al. Bioethics for Children: Involving Children in Medical Decisions.
†Source: U.S. Cancer Statistics Working Group. United States Cancer Statistics: 1999–2011 Incidence and Mortality Web-based Report. Atlanta (GA): Department.
Ad Hoc Committee Update: Impact of NCAA Sickle Cell Trait Mandate Alexis Thompson January 16, 2014.
Doug Altman Centre for Statistics in Medicine, Oxford, UK
Ethical AND legal issues in GENETICS. objective 1- introduction. 2-major needs in study of ethics. 3-Ethical Principles in Medicine. 4-The Special Position.
Developing information for participants in your research – getting started This presentation contains some exercises to help you get started. You can do.
Copyright © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins Chapter 1 Overview of Nursing Process, Clinical Reasoning, and Nursing Practice.
A PARTNER YOU CAN TRUST. WHO HAS A REASSURING COMBINATION FOR PARENTS AND CHILDREN?
1 Consent for treatment A summary guide for health practitioners about obtaining consent for treatment Bridie Woolnough Resolution Officer Health Care.
What is personal genetics? What might it mean for me, my family and society? Personal Genetics Education Project (pgEd) Harvard Medical School
E THICS IN P SYCHOLOGY Ethics Committee Role of the Researcher Participant’s Rights.
Implementing the School Health Index in Your School A discussion of the benefits of the School Health Index tool.
Clinical Trials. What is a clinical trial? Clinical trials are research studies involving people Used to find better ways to prevent, detect, and treat.
GENETIC TESTING: WHAT DOES IT REALLY TELL YOU? Lori L. Ballinger, MS, CGC Licensed Genetic Counselor University of New Mexico Cancer Center.
Obesity a Growing Problem! CAPT Martha Culver Acting Deputy Regional Administrator Nurse Consultant CDR Madelyn Reyes Senior Nurse Consultant Health Resources.
Adult-Onset Disease The Example of Colon Cancer Summer, 2012.
Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection DR. S.K CHATURVEDI DR. KANUPRIYA CHATURVEDI.
Vocabulary quiz in 5 minutes! Also, have your definitions sheet ready with your name on it to hand in!
Attention-Deficit Hyperactivity Disorder (ADHD or AD/HD) & Medication Group 5: Kristy O'Donoghue, Julie Savage, Rachel Thayer & Jaclyn Zoll.
Integrated Approach towards Investing in Children
Evaluation of the Indiana ECCS Initiative. State Context Previous Early Childhood System Initiatives –Step Ahead –Building Bright Beginnings SPRANS Grant.
Consent Procedures. What is Informed Consent? Consent by a patient to a surgical or medical procedure or participation in a clinical study after achieving.
Introduction to Healthcare and Public Health in the US The Evolution and Reform of Healthcare in the US Lecture b This material (Comp1_Unit9b) was developed.
1 Ethical Issues in the Care of PLHIV HAIVN Harvard Medical School AIDS Initiatives in Vietnam.
Ethical AND legal issues in GENETICS. objective 1- introduction. 2-major needs in study of ethics. 3-Ethical Principles in Medicine. 4-The Special Position.
Objective 9/23/15 Today we will be completing our research methods unit & begin reviewing for the upcoming unit assessment 9/25. Agenda: -Turn in all homework.
Child Protection Services Department of Health and Human Services Maggie Crawford State Manager Child and Family Services 3 April 2006.
Talking to Your Family About Your Diagnosis of Hereditary Breast and Ovarian Cancer Syndrome Several of my aunts died of breast cancer, so I was very worried.
1115 Waiver Proposals California Children’s Services Program.
Implementing NICE guidance on autism – developing a local autism team January 2014 Autism: the management and support of children and young people on the.
Health Care Self-Management (Provider Version) Late Effects of Treatment for Childhood, Adolescent and Young Adult (AYA) Cancers Supported by a grant from.
Provider Initiated HIV Counseling and Testing Unit 2: Introduction and Rational for PIHCT.
Medical Necessity Criteria An Overview of Key Components Presented by BHM Healthcare Solutions.
Causes of Down's Syndrome
What are some benefits, risks and limitations of genetic testing?
Genes in Life is a place to learn about all the ways genetics is a part of your life. On this site you will learn:   How.
Communicating Science Thomas Workman, Ph.D. American Institutes for Research AIR American institutes for research logo Asterisk after silde indcates to.
Introduction: “Please write down everything that comes into your head when you hear the words ‘DNA risk tests’” Colorectal cancer Type 1 diabetes Information.
Health – related behavior
Summary and Conclusion:
Week 5: Ethical, Legal & Social Issues in Applied Genomics
Secondary findings from Genome-wide Testing
1st International Online BioMedical Conference (IOBMC 2015)
Gene Editing: Ethics and Governance
Professor of Community Genetics and Public Health Genomics
Huntington’s Chorea By Alyce & Ryan.
Food Allergies: Diagnosis & Management
WHY GENETIC COUNSELING IS IMPORTANT
Themes and perspectives in safeguarding theory
EPHA – PE & School Sport presentation.
Session 1: The Importance of Costing VAW
Genetic testing and screening are two different things.
Diagnosis of disease M2/D2
Biology and Your Future
Assignment 2 Learning Aim D: Individual Treatment Plan
Public Health Initiatives Estonia
Component 1: Introduction to Health Care and Public Health in the U.S.
A person’s genome is his/her complete set of DNA
Most provincial and territorial health insurance programs cover prenatal blood screening for chromosomal anomalies (Down syndrome and Trisomy 18) and neural.
Medical geneticists are physicians who, after finishing their medical degree, receive specialist training in genetics through one or more of the following:
No matter what the type of genetic screening, certain core principles should be followed before a program is introduced. Principles of Screening • The.
Prenatal genetic screening is intended to provide information about the health of the fetus.  Prenatal screening can bring to light serious disabilities,
Nuchal translucency screening uses ultrasound to screen for Down syndrome, other conditions caused by an extra chromosome (trisomy 13 and 18), and congenital.
Six W’s of Genetic Testing
Public Health Initiatives Estonia
Presentation transcript:

Diagnostic testing is genetic testing to diagnose a childhood condition or conditions that can be treated medically during childhood. An example is retinoblastoma (a cancerous tumour of the eye). These tests are done in order to access treatment or management of a suspected genetic condition, where the treatment is likely to positively impact the child’s condition. Genetic testing is offered if a child has symptoms and the test is used to confirm a medical diagnosis. There are also true predictive testing situations where genetic testing will enhance monitoring, treatment, or prevention in a healthy child at risk for a genetic condition but who does not have symptoms.1 The Canadian Paediatric Society (CPS) and the Canadian College of Medical Geneticists (CCMG) have developed guidelines for genetic testing of children. Highlights of the Guidelines for Genetic Testing of Healthy Children1 • The best interests of the child should be the primary consideration when contemplating testing.  • Parents should be informed of potential psychological and social risks associated with testing. • There should always be appropriate counselling and genetic service involvement. • Timely medical benefit to the child should guide genetic testing.  • When genetic conditions will not present until adulthood, testing should be delayed until the child is competent to decide whether they want the information. • When carrier status for conditions is important only in reproductive decision-making, testing of children should be discouraged until the child is able to participate fully in the decision to be tested. • Clinicians should consider requests for genetic testing by competent, well-informed adolescents for the purpose of reproductive decision-making. For the full set of recommendations go to this site: http://www.cps.ca/documents/position/guidelines-for-genetic-testing-of-healthy-children 1Arbour L. Guidelines for genetic testing of healthy children. A joint statement with the Canadian College of Medical Geneticists Bioethics Committee, Canadian Paediatric Society (CPS) Ethics and Public Policy Committee, Canadian College of Medical Geneticists. Paediatrics & Child Health. 2003;8(1):42–5. Reference No. B03-01. Reaffirmed January 2011. Addendum April 2008.