48,XXYY Syndrome
What is 48,XXYY Syndrome ?
48,XXYY syndrome is a rare genetic condition caused by a chromosome aneuploidy.
48,XXYY syndrome is a rare genetic condition caused by a chromosome aneuploidy.
48 XXYY syndrome is diagnosed either by prenatal testing during pregnancy or by a blood test which examines the chromosomes (karyotype) of the patient.
Last updated 15 Apr 2009, 05:09 PM
15 Apr 2009, 05:09 PM
Men with XXYY are considered infertile. There are no documented cases of a male with XXYY producing a child using natural methods. If you are looking to get pregnant, Dr Paduch (http://www.weillcornell.org/dpaduch/) has been doing some pioneering work with sperm extraction. I would recommend that you contact him to see if there is a possibility that his procedures might be successful for your case.
15 Apr 2009, 04:44 PM
My Current boyfriend has xxyy, is infirtillity 100% or is there a small chance that he can reproduce
16 Dec 2008, 01:49 AM
The mission of the XXYY Project is to build the capacity of parents and service providers to assist males with XXYY in leading purposeful, productive lives. If you want to learn more about 48 XXYY Syndrome, please contact The XXYY Project: The XXYY Project PO Box 460625 Aurora, CO 80046-0625 Phone: (303) 400-3456 Fax: (303) 400-3454 http://xxyysyndrome.org
| Title | Description | Date | Link |
|---|---|---|---|
| The XXYY Project |
The mission of the XXYY Project is to build the capacity of parents and service providers to assist males with XXYY in leading purposeful, productive lives.
The XXYY Project PO Box 460625 Aurora, CO 80046-0625 Phone: (303) 400-3456 Fax: (303) 400-3454 |
03/20/2017 |
Clinical Trials
CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access.
Enrolling is easy.
- Complete the screening form.
- Review the informed consent.
- Answer the permission and data sharing questions.
After these steps, the enrollment process is complete. All other questions are voluntary. However, these questions are important to patients and their families to create awareness as well as to researchers to study rare diseases. This is why we ask our participants to update their information annually or anytime changes to their information occur.
Researchers can contact CoRDS to determine if the registry contains participants with the rare disease they are researching. If the researcher determines there is a sufficient number of participants or data on the rare disease of interest within the registry, the researcher can apply for access. Upon approval from the CoRDS Scientific Advisory Board, CoRDS staff will reach out to participants on behalf of the researcher. It is then up to the participant to determine if they would like to join the study.
Visit sanfordresearch.org/CoRDS to enroll.
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The XXYY Project
Created by batthish | Last updated 15 Apr 2009, 05:09 PM
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