help@rarechromo.org
Helpline: +44 (0) 1883 723356
Understanding Rare Chromosome and Gene Disorders
DONATE JOIN US
  • Families
  • Professionals
  • Support Us
  • Shop
  • Who we are

EXISTING MEMBER LOGIN

LOGIN

Forgot password? Please contact us membership@rarechromo.org

Registered member but first time log in? Just go to the Unique Members Area Registration Form

Not yet a registered member? Just go to the Become A Member page

close

About Us

  • Our History
  • Legal Status
  • Annual Reports
  • Funding Sources
  • Disclaimer
  • Resources
  • Equal Opportunities Policy
  • Data Protection & Privacy Policy
  • Advertising Policy
  • Accessibility
  • Cookie Policy
  • Terms & Conditions
  • Get in Touch
Log In

Contact Us

help@rarechromo.org
Helpline:
+44 (0) 1883 723356

Fundraising & Admin:
+44 (0) 1883 723306

Address:
The Stables, Station Road West
Oxted
Surrey
RH8 9EE
UK
Find us here

Sign Up

Our Twitter

FOLLOW US

Unique

@unique_charity ·
22 Aug

It’s #SATB2-Associated Syndrome (SAS) Awareness Day!
Our guide is designed to help families and healthcare professionals looking after people with SAS. It contains information about the cause, how it can affect people and how to manage this condition.

https://rarechromo.org/media/information/Chromosome%20%202/SATB2%20syndrome%20FTNW.pdf

2

Unique

@unique_charity ·
21 Aug

It’s #DYRK1Asyndrome Awareness Day!

Did you know? The Deciphering Developmental Disorders, is seeking to identify genetic causes of developmental delay in children and has identified DYRK1A as being one of the 10 most frequent genes involved. https://rarechromo.org/media/information/Chromosome%2021/DYRK1A%20and%2021q22.13%20deletion%20syndrome%20FTNW.pdf

Unique

@unique_charity ·
21 Aug

It’s #DYRK1Asyndrome Awareness Day!

Our guide is designed to help families and healthcare professionals looking after people with DYRK1A syndrome. It contains suggestions about the help and management of the condition.

Take a look: https://rarechromo.org/media/information/Chromosome%2021/DYRK1A%20and%2021q22.13%20deletion%20syndrome%20FTNW.pdf

Follow Us

Copyright © 2026 Unique
Site editor Sarah Wynn PhD
Rare Chromosome Disorder Support Group. Registered charity no. 1110661
Designed by Caravan
Clinical photography provided by St George's University Hospital
close