banner
 
bar

program

  test
bar
 
 

GeneticScreeningWRAP:

Prenatal Screening for Genetic Disorders

MedicineWRAP CME Disclosure

Please read this notice and click the acknowledgement
at the bottom of the page to continue.

Program Medium:

Internet-based program

Method of Physician Participation Utilized in Learning Process:

There are no fees for participating and receiving CME credit for this activity. During the period April 1, 2010 through April 1, 2012 participants must 1) read the learning objectives and faculty disclosures; 2) study the educational activity; 3) register and complete the evaluation form; and 4) print out your CME certificate.

Estimated Time to Complete Educational Activity:

Two hours

Course Overview:

In this web-based program, physicians will learn how recent advances in basic and clinical research have helped to advance strategies for prenatal screening for genetic disorders, and review evidence-based approaches and guidelines for screening for cystic fibrosis, trisomies, Fragile X and SMA.

Release Date:

April 10, 2010

Expiration Date:

April 10, 2012

Intended Audience:

  • Obstetricians
  • Gynecologists
  • Primary care physicians
  • Family medicine specialists
  • Geneticists
  • Pediatricians
  • Genetic counselors
  • Nurse practitioners
  • Physicians assistants

Registration:

Enrollment for this MedicineWRAP is complimentary, and clinicians are invited to participate in this CME-certified WebCAST and/or share this invitation with other colleagues, departmental staff members, and healthcare professionals.

Grantor Support:

Boehringer IngelheimSupported by an independent educational grant
from Quest Diagnostics.

Accreditation Statement:

This activity has been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education through the joint sponsorship of The University of Massachusetts Medical School, Office of CME and CMEducation Resources, LLC. The University of Massachusetts Medical School is accredited by the ACCME to provide continuing medical education for physicians.

Credit Designation Statement:

The University of Massachusetts Medical School designates this educational activity for a maximum of 3.0 AMA PRA Category 1 Credit(s). Physicians should only claim credit commensurate with the extent of their participation in the activity.

Policy on Faculty & Provider Disclosure:

It is the policy of the University of Massachusetts Medical School to ensure fair balance, independence, objectivity and scientific rigor in all activities. All faculty participating in CME activities sponsored by the University of Massachusetts Medical School are required to present evidence-based data, identify and reference off-label product use and disclose all relevant financial relationships with those supporting the activity or others whose products or services are discussed. Faculty disclosure will be provided in the activity materials.

Program Faculty and Disclosures:

Wayne W. Grody, MD PhD
Professor and Director
Diagnostic Molecular Pathology Laboratory
Department of Pediatrics and Human Genetics
David Geffen School of Medicine at UCLA
Los Angeles, California

Nothing to disclose

Program Managers and Web Editor Disclosure:

Program Manager Gideon Bosker, MD has nothing to disclose.

Program Reviewers Denise Leary and Richard Aghababian, MD have nothing to disclose.

Educational Objectives:

Participants in this CME-certified MedicineWRAP will:

  • Learn appropriate, guideline-consistent strategies for prenatal maternal serum screening for cystic fibrosis, aneuploidies, Fragile X and spinal muscular atrophy (SMA)
  • Learn how to utilize recommended, guideline-consistent prenatal genetic screening tests based on practice guidelines from ACOG and the ACMG
  • Learn how to counsel families about the results and implications of prenatal genetic screening diagnostic tests
  • Learn how to employ prenatal screening tests for specific ethnic and racial groups, based on their risk for specific disorders
  • Learn about the ethical and practical implications of prenatal maternal screening for genetic disorders
  • Learn how to appropriately utilize core panels for CF, and indications for screening for Fragile X syndrome and SMA

Hardware and Software Requirements:

To participate in this program, viewers must have a PC or Macintosh computer that has active, ongoing internet access for the duration of the program, as well as a compatible Flash-viewer. An email address is required for registration, and a printer is required to printout the CME certificate.

Privacy Policy

When you participate in a CME activity offered by CMEducation Resources, we ask you for your name, degree, affiliation, street address, telephone number, fax number, and/or e-mail address (the "Information"). We use that Information in the following ways:

  • We use the Information to grade your post-test and to send you a certificate of completion of the CME activity. If we use a third-party company to grade your post-test and issue certificates of completion, we will give the Information to that company for that purpose only.
  • For each CME activity that you take, you must complete an evaluation questionnaire. That questionnaire asks if you are willing to participate in a follow-up survey. If you answer yes, we will use your name and contact information to send you the survey.
  • We may use the Information to send you information about other CME activities that CMEducation Resources is offering.
  • If our company is acquired by or merged into another company, we may make the Information available to the new owner/entity to use in the ways described above, to enable it to continue our business.
  • You should check this privacy policy periodically to see whether we have made any changes.

Disclaimer:

Copyright © 2011 Resources, LLC All rights reserved.

Reproduction, distribution, or translation without express written permission is strictly prohibited.

Content on this webcast reflects the opinions, output, and analyses of experts, investigators, educators, and clinicians whose activities for, while independent, are commercially supported by the sponsor noted at the start of each activity.

Content on this webcast is not meant to be, nor substitute for national guidelines or recommendations generated by professional, academic societies, colleges, or associations.

Content on this webcast is intended for educational value only. Its contents, analyses, and any recommendation made herein are intended to make scientific information and opinion available to health professionals, to stimulate thought, and further investigation. This webcast is not designed nor is any aspect of the contents here intended to provide advice regarding medical diagnosis or treatment for any individual case. Any decisions regarding diagnosis and/or management of any individual patient or group of patients should be made on individual basis after having consulted appropriate sources, whether they be appropriate consultants and/or guidelines and recommendations issued by national organizations, professional societies, governmental health organizations, or similar bodies. This webcast is not intended for use by the layman.

Opinions expressed herein are not necessarily those of CMEducation Resources, LLC, program supporters or accreditors, but reflect the opinions and analyses of the experts who have authored the material. Mention of products or services does not constitute endorsement. Clinical, legal, financial, and other comments are offered for general guidance only; and professional counsel should be sought for all specific situations.

bar

program

  test
bar

I have read this CME information statement and wish to participate in this CME activity.

Copyright © 2011 Resources, LLC All rights reserved.

 
6

 

Key Program Topics Include:

ACMG
ACMG/ACOG
ACOG
advanced maternal age
AFP
Ashkenazi
Bloom syndrome
Canavan disease
Carrier Screening
chromosome abnormality
Chromosome Analysis

Chromosome Disorders
Connexin-26 deafness
Cystic Fibrosis
diagnosis
diagnostic
Down syndrome
Familial dysautonomia
Familial Mediterranean fever
Fanconi anemia
fetal lymphocytes

 

FMR1allele
Fragile X
Gaucher disease
Genetic
genetic disorder
genotype
hCG
Maternal age
mRNA
Mutation Panels
Niemann-Pick disease
NTD
phenotype
Population screening
premutation
tremor-ataxia-dementia
Prenatal Diagnosis
sequencing
Tay-Sachs
Triple Marker Screen
trisomies
trisomy 18
uE3