The UNIQUE - The Rare Chromosome Disorder Support Group is a non-profit, voluntary organization dedicated to promoting awareness of rare chromosomal abnormalities. One of the Unique helpline team (Beverly, Arti, Sarah or Francesca) will respond within 7 days with your membership number, so please watch out for our reply email (including your spam folder!).

A couple of other rare genetic disorders have also been linked to mutations in the aforementioned gene. Unique is a registered charity (Registration no.

Guides to some autosomal dominant single gene disorders can be found on a separate page .

This condition is caused by mutations in WAS gene located on the X chromosome. Unique is a registered charity (Registration no. 1110661). Our mission is to inform, support and alleviate the isolation of anyone affected by a rare chromosome or autosomal dominant single gene disorder and to raise public awareness. The organization was founded in 1984 and served as a source of support and information for anyone affected by any rare chromosome abnormality.

Our mission is to inform, support and alleviate the isolation of anyone affected by a rare chromosome or autosomal dominant single gene disorder and to raise public awareness. Wherever you are in the world, you are not alone on this journey. Information on genetic changes is a very fast-moving field and Unique does its best to keep abreast of changing information and to review its published guides as needed. This study is a collaboration between Unique and the Centre of Expertise for Rare Chromosome Disorders – University Medical Centre (UMC) Groningen, the Netherlands. Unique is a source of information and support for families and individuals affected by rare chromosome disorders.

Chromosome guides are listed under the relevant chromosome number. This organization is based in the United Kingdom, but welcomes members worldwide. The email with the link to the survey will be sent by researchers at the Expertise Centre.

1110661). Unique also has a list of Registered Chromosome Disorders. Treatments for WAS are currently symptom(s) based i.e treating symptoms as they arise.