[ASD Related Information] Genetic Disorder and ASD - 16p11.2 microdele…
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[ASD Related Information] Genetic Disorder and Autism Spectrum Disorder (ASD)
※ 16p11.2 microdeletions syndrome
It is a disease that causes various symptoms due to the loss of genes in the corresponding area due to the microdeletion of the proximal end near the central section of chromosome 16. It is found in 1 in 300 ASD children. Along with ASD, developmental delay or intellectual disability, speech delay, head size increase, and overweight can occur.
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