The 8th International Symposium on MPS and Related Diseases will be held in Mainz, Germany. Traditionally, this symposium unites scientists, patients and their parents to share and discuss recent scientific results.

National coalition of consumers, professionals, and genetic support groups to voice the common concerns of children, adults, and families living with, and at risk for, genetic conditions.

A discussion board for those affected by BCM. Read the contents, search and post from this location.

A support and awareness discussion board for people affected by this disorder.

Support group for families who have children with any chromosome 22 disorder, including trisomies, cat eye syndrome, translocations, deletions 22q11, 22q13, VCFS, Digeorge syndrome, rings and unique malformations.

Non-profit voluntary support group for families affected by rare chromosome disorders.

Information on rare chromosomal disorders. Support and advice for families.

Family support organization which exists to ensure the early and accurate diagnosis of CdLS, promote research into the causes and manifestations of the syndrome, and help people with a diagnosis of CdLS, and others with similar characteristics, make informed decisions throughout their lifetime.

Support for families of children with Distal Trisomy 10q. Family stories, contacts, other information.

A forum for sharing information, increasing public awareness, and building advocacy for further research for patients diagnosed with Myotonic Dystrophy Type 2.

A support group for families and professionals interested in the chromosomal condition known as isodicentric 15 (formerly inverted duplication 15).

This is a discussion group about lafora body disease.

Sites are listed alphabetically by disease/condition.

Resources, articles, support and general information on the rare disorder, Oto-Palatal-Digital Syndrome.

A support board for those parents of children born with extra toes/fingers as well as webbing. A place to learn new information and make friends with others

An online support group for people dealing with Peter's Anomaly.

The Philadelphia, PA., Internetsupport For invisible/hidden disabilities.

A United Kingdom support organisation for parents of infants with Trisomy 13 and 18 and other related disorders.

Support Organization in the United States for Trisomy 18, 13, and other related disorders. Provides literature, conferences, newsletter, chapter information, and international contacts.

A forum for people who have chromosome abnormalites to show support, give advice and comfort.

This is a memorial website for Thomas Scott Davidson who died from Anencephaly.

This site was made in memory of our daughter Abigail Renee, to help other families who have been given a diagnosis of Trisomy 18.

A place to list your Trisomy 18, Edwards syndrome memorial site , get help making a website, to share your unique story via the web.

Participate in this support group for those pregnant with, parenting, or grieving the loss of child with Trisomy 18. Includes resources for all stages of the journey.

Support and information for families of children with rare disorders.

The mission of the European Porphyria Initiative (EPI) is to present an up to date approach to the understanding of porphyria.

Features a Yahoo! group for family support for individuals caring for others affected by "Alpha Thalassemia Mental Retardation Syndrome (ATR-X).

An active support site for the parents and families of children with Floating Harbor Syndrome.

A very active support group that prides itself on helping its members through the good - bad days and posting the latest CMT/HMSN/HNPP research information available on the web.