Radio-Tartaglia Syndrome: A Rare Cause of Delay in Neurodevelopment - A Case Report
Background: Radio-Tartaglia syndrome or RATARS is an unfamiliar disease caused by a heterozygous mutation of the SPEN gen in the 1p36 chromosome. Clinically, it is represented by global developmental delay and intellectual disability; however, it can also be associated with other relevant comorbidit...
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Main Authors: | Maria Arteaga Pichardo (Author), Felipe Bernate (Author), Juan Trujillo Angel (Author), Maria Santana Alba (Author), Maria Lubo (Author), Natalia Avellaneda Perdigon (Author), Lev Bladimir Ramirez (Author), Daniel Jimenez (Author), Sofia Atuesta Escobar (Author), Isabel Fernandez Gonzalez (Author), Luis Celis Regalado (Author) |
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Format: | Book |
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Mashhad University of Medical Sciences,
2024-07-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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