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University of Iowa
Division of Medical Genetics
Testing Protocols
Patients Name
Hospital Number
DOB
Presymptomatic Testing for Huntington Disease / Informed Consent
I _____________________________________choose to
participate in presymptomatic testing for the presence of the Huntington disease (HD) gene. I
have been told that I am at risk for HD because there is a history of this disorder in my family.
I understand genetic material will be evaluated only for the gene change responsible for HD and
will not be used for any other testing. This test will most likely tell me if I have or have not
inherited the gene that causes HD.
I understand I must participate in a testing protocol
that provides genetic counseling and any necessary follow up care. I agree to participate in the
minimum of three counseling sessions required for the testing. There will be at least two
sessions prior to the test result session. Sessions will last 1-3 hours. These sessions will
include information about HD, genetic testing, consequenses of results and available support
services.
I understand a neurological exam is recommended. I am
aware this examination may disclose that I have clinical signs of HD and I will be told of my
results.
I understand the test does have some limitations.
First, it is not known if everyone who is affected with HD has the same change in the gene
causing the disease. Second, occasionally the result of gene analysis cannot be interpreted with
confidence.
I understand there can be three outcomes to the test:
1. The gene change in my Family might not be
interpretable, so my test results will not tell me more than I know now.
2. I do not have the HD mutation.
3. The HD gene mutation is present and I will develop
HD.
I understand my participation in this program is
voluntary and I can terminate my participation at any time without jeopardy to my medical care.
I understand if at any time my continued participation in this program is considered injurious
to my health or disadvantageous to me, the testing staff may recommend postponement of the testing.
The information provided is technical and receiving it
will be stressful. Because of this, I am encouraged to bring a close friend, spouse, or other
family member not at risk for HD to accompany me through the test procedures. I understand the
professionals involved in this testing are willing to answer my questions and to discuss my
concerns with me throughout the testing procedure. Counselors will assist me in arranging for
any additional professional counseling and support I may need.
Risks of this testing include:
A. concerns of a psychological nature. I understand
the testing may be lengthy and does require a waiting period before results are available. These
events may cause me to confront difficult psychological issues. Since I may withdraw from the
testing protocol at any time and the process is a long one, decisions about my continued
participation may evoke anxiety. An uninterpretable result can be frustrating and can intensify
the ambiguity of the risk situation. Knowing I do not have the common mutation for HD can produce
mixed emotions. I may also have to confront the fact I have inherited the mutation that causes
HD and will develop the disease. I am aware the testing cannot predict when I first will show
signs of HD nor can it predict the severity or rate of progression of HD. This will also mean
that my children will have a 50% chance of inheriting the HD mutation.
B. possible difficulties with employment or insurance.
C. discomfort of a blood draw and a bruise. I
understand this test requires me to provide 20cc (two tubes) of my blood.
D. financial liability. I will be responsible for the
costs of the laboratory testing and counseling regardless of the outcome of my testing. In some
cases, medical insurance will not pay for this testing.
I understand results of my testing will not be
available to any one other than the professionals involved and is not to be released to any
second party without my written consent.
Test results will be given only to me and only in person.
_________________________________has explained to me
the purposes of the testing protocol and I agree to participate in this testing program. I
acknowledge the possible risks, discomforts, and benefits I may experience. I have read and I
understand this consent form.
__________________________________________________________________
Participant Date
__________________________________________________________________
Witness to Signature Date
Copyright 1997, University of Iowa, Division of
Medical Genetics
Copyright © 2010, ISONG |