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SETBP1 Society
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    • Newly Diagnosed
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Month: January 2022

New Documented SETBP1-HD and SETBP1-Related Disorders Dashboard

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New Documented SETBP1-HD and SETBP1-Related Disorders Dashboard

by haley / On January 24, 2022Posted in Research, Resources

SETBP1 haploinsufficiency disorder (SETBP1-HD) is an ultra rare, genetic neurodevelopmental disorder. SETBP1-HD is caused by a loss-of-function change on one copy of the two copies of the SETBP1 gene. There are also some changes on one copy of the SETBP1 gene where we do not know how the SETBP1 function is impacted. For changes where […]

What is SETBP1?

SETBP1 haploinsufficiency disorder is a very rare disorder that is the result of a loss-of-function of one copy of the SETBP1 gene and causes a spectrum of symptoms ranging from absent speech to expressive language delays, mild-severe intellectual disability, autistic-traits or autism, developmental delays and ADHD.

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SETBP1 Haploinsufficiency Disorder guide >

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