Pediatric CMA Patient Brochure-112014-FINAL-Low-Res

For more information, visit
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Peace of Mind for Patients
At Progenity, we believe all patients should
have access to the highest-quality genetic tests
without the burden of exorbitant medical costs.
That’s why we offer the Peace of Mind program,
which provides payment assistance for patients
who are facing financial difficulties. To discuss
your options, please call us toll-free at
+1 855-293-2639, option 4.
Chromosomal Microarray Analysis
5230 S. State Road, Ann Arbor, MI 48108
Tel +1 855-293-2639
progenity.com
Progenity is a CLIA-certified clinical laboratory and
is accredited by the College of American Pathologists
(CAP). The information contained in this brochure is
provided by Progenity as an educational service for
physicians and their patients.
© 2014 Progenity, Inc. All rights reserved.
Progenity® is a registered service mark of Progenity, Inc.
REV 112014
For Pediatric
Genetic Testing
What is Chromosomal
Microarray Analysis?
What can I learn from the
results of this test?
Chromosomal Microarray Analysis (also called
CMA) is a test that looks for extra or missing
genetic information. We all have changes
in our genetic information, or DNA. These
changes shape how we grow and develop. Some
of these gene changes cause differences like
hair and eye color; while other changes can be
associated with health and/or developmental
problems as the child grows.
If the test detects a genetic change associated
with health problems, this may help your
healthcare provider diagnose the condition,
which could help you better understand
your child’s condition. It may be easier to
understand future health problems and may
help predict what to expect as your child
gets older. It also may allow you and your
healthcare providers to work together to give
your child specialized medical care at an
earlier age in order to maximize his or her
potential. This information may also help
at-risk family members to seek genetic testing
and aid in future family planning.
Why should I consider this
test for my child?
Your provider may recommend CMA testing if
your child has problems with learning, physical
development, has birth defects or had previous
genetic testing like chromosome analysis with
negative results. This test may help determine
if a genetic change is the cause.
How is the test performed?
A small blood sample is collected from the
child and is sent to the lab for analysis. The lab
will issue a report of findings to the healthcare
provider who ordered the test. Your healthcare
provider will then discuss these results with
you, and together you can decide on the next
steps for your child’s health care.
If the test does not detect a genetic change
associated with health problems, then your
healthcare provider may recommend
further testing.