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General Information
Background Information
How Rare is SAS
What Causes the Syndrome
Understanding Genetic Testing Results
Main Characteristics
Making the Diagnosis
For Professionals
Medical Journal Articles
List of Mutations (Published and public databases)
Recommended Screening Guidelines
How to Help
Resources
Contact Us
Home
General Information
Background Information
How Rare is SAS
What Causes the Syndrome
Understanding Genetic Testing Results
Main Characteristics
Making the Diagnosis
For Professionals
Medical Journal Articles
List of Mutations (Published and public databases)
Recommended Screening Guidelines
How to Help
Resources
Contact Us
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Resources
Helpful Links
A brochure made by
Unique
(
rarechromo.org
) dedicated to
SATB2
-associated syndrome and that complements the information found on this website can be found here:
http://www.rarechromo.org/information/Chromosome%20%202/SATB2%20syndrome%20QFN.pdf
A brochure made by
Unique
(
rarechromo.org
) dedicated to deletions of 2q33.1 and that complements the information found on this on this website can be found here:
http://www.rarechromo.org/information/Chromosome%20%202/2q33.1%20deletions%20and%20other%20deletions%20between%202q31%20and%202q33%20FTNW.pdf
There are several Facebook support groups that encompass patients with deletions, duplications or mutations of the
SATB2
gene:
“SATB2 syndrome (2q31-2q33) and Glass Syndrome”:
https://www.facebook.com/groups/185098831860332/