Searching for Xyy Support information? Find all needed info by using official links provided below.
https://rarediseases.org/rare-diseases/xyy-syndrome/
A diagnosis of XYY syndrome is made based upon a thorough clinical evaluation, a detailed patient history, and specialized tests (i.e., chromosomal analysis) that detect the presence of an extra Y chromosome (47,XYY karyotype). A diagnosis of XYY syndrome may be made before birth (prenatally) through amniocentesis or chorionic villus sampling ...
The Association for X and Y Chromosome Variations (AXYS) is dedicated to addressing the needs of those affected by one or more extra X and/or Y chromosomes. We are focused on sharing knowledge, offering support, and initiating action to help improve lives of individuals and families.
https://rarediseases.info.nih.gov/diseases/5674/47-xyy-syndrome
35 rows · Jan 14, 2018 · 47, XYY syndrome is a syndrome (group of signs and symptoms) that affects …
https://genetic.org/im-parent-affected-child/support-groups/
Support groups can meet in homes, public meetings spaces at libraries or churches and synagogues, or in community rooms at hospitals. Many support groups have found that a meetings with a speaker and group discussion, and social events such as picnics or meetings at …
https://ghr.nlm.nih.gov/condition/47xyy-syndrome
Oct 29, 2019 · 47,XYY syndrome is characterized by an extra copy of the Y chromosome in each of a male's cells. Although many males with this condition are taller than average, the chromosomal change sometimes causes no unusual physical features.
https://rarediseases.info.nih.gov/organizations/3813
If you have problems viewing PDF files, download the latest version of Adobe Reader. For language access assistance, contact the NCATS Public Information Officer. Genetic and Rare Diseases Information Center (GARD) - PO Box 8126, Gaithersburg, MD 20898-8126 - Toll-free: 1-888-205-2311
https://www.facebook.com/groups/47XYYSYNDROMESUPPORT/
47 XYY SYNDROME SUPPORT GROUP has 722 members. This is a group for Males, Parents/Carers and relatives of Males with XYY Syndrome to come together for...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4097881/
Subjects were recruited to the Philadelphia XYY study from a broad geographic and socioeconomic distribution through the support of the national XYY advocacy organization, by direct referral through an established referral network of university- and community-based pediatricians, and through the genetics clinic at A.I. duPont Hospital for Children.Cited by: 73
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