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Baylor College of Medicine

Rett Syndrome, MECP2 Duplication Disorder, and Rett-Related Disorders

Description

Content

This study is looking at patients’ with Rett syndrome, MECP2 duplication, FoxG1, CNKL5 and family history related to Rett syndrome and MECP2 mutation.

The study is available to patients ages 0-65+ years old with diagnosis of Rett syndrome, MECP2 duplication, FOXG1 and CDKL5.

Contact:

Jackie Soto
Phone: (832) 822-1260
Email: jxsoto@texaschildrens.org

Contact

Jackie Soto

Phone 1: 832–822–1260

Phone 2: 832–822–1260

IRB: H-36995

Status:

Active

Created:

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