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  • A syndrome that has_material_basis_in genetic changes that affect the SATB2 gene and that is characterized by mild to severe intellectual disability, a delayed or absent ability to speak, severe speech anomalies, abnormalities of the palate, teeth anomalies, behavioral issues with or without bone or brain anomalies, and onset before age 2.
database_cross_reference
  • url:https://ghr.nlm.nih.gov/condition/satb2-associated-syndrome
  • url:https://www.ncbi.nlm.nih.gov/books/NBK458647/
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