THE MED13L FOUNDATION INC

The MED13L Foundation

Supporting MED13L families through awareness, research, and community. Connecting hearts and minds to overcome challenges. #NDD #Epilepsy #Autism #ID 🧬💙🧠 The MED13L Foundation is a registered 501(c)(3) nonprofit. Our ICD-10 Code is Q87.85. Update your provider today! We exist to help support MED13L families by Communicating, Connecting and Empowering!
822469441
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2017
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BARRINGTON, NJ 08007
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med13l.org
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Families Supporting the MED13L Syndrome Cause. We strive to spread awareness provide family support and advance medical research in search of a cure for MED13L syndrome. MED13L Syndrome A Rare Genetic Neurodevelopmental Disorder MED13L Syndrome was first described as a neurodevelopmental disorder in 2013. It was further expanded by both Adegbola and Asadollahi as a Syndrome with global developmental delay intellectual disability ID with speech and movement delay hypotonia low tone and recognizable facial features.

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