Genetic Disorders Support Resources
The Turner Syndrome Society of the US / New Jersey Chapter
The goal of the Turner Syndrome Foundation (TSF) is to support research initiatives and develop programs for education - information - support, which will increase professional awareness and enhance medical care of those affected by Turner syndrome. Early diagnosis and comprehensive treatments over the lifespan will lead to a brighter and healthier future for all young girls and women with Turner syndrome. TSF is a registered 501(c)3 organization incorporated in New Jersey, EIN #27-1409942.
Turner Syndrome Foundation, Inc.
P.O. Box 726, Holmdel, NJ 07733
732-217-3021 / Toll Free: 800-594-4585 / Fax: 800-594-3862.
The FXANJ is an association of families and professionals dedicated to improving the lives of those living with Fragile X syndrome. For more information visit
The goals of the New Jersey Rett Syndrome Association (NJRSA) are to contribute towards an improved quality of life for girls and women affected by Rett Syndrome, raise awareness of the disorder and support research for a treatment and cure. By raising the awareness we foster public attitudes conducive to early intervention, treatment, support and research of Rett Syndrome. NJRSA is a 501(C)3 organization.