Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”
<p dir="ltr">Autism spectrum disorder (ASD), a neurodevelopmental illness that affects children at an early age with a global prevalence of 1%, is diagnosed based on clinical features such as social impairment, repetitive behaviors, and restricted interests. ASD is genetically hetero...
محفوظ في:
| المؤلف الرئيسي: | |
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| منشور في: |
2023
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| الموضوعات: | |
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إضافة وسم
لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!
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| الملخص: | <p dir="ltr">Autism spectrum disorder (ASD), a neurodevelopmental illness that affects children at an early age with a global prevalence of 1%, is diagnosed based on clinical features such as social impairment, repetitive behaviors, and restricted interests. ASD is genetically heterogeneous, and the genetic etiology of ASD remains unknown in 20–60% of autistic people. ASD subjects commonly have co-occurring comorbidities such as intellectual disability (ID), seizures, sleep problems, or digestive problems, which suggest more complex genetic etiologies. Exome sequencing and other next-generation sequencing (NGS) techniques have been successful in increasing the total number of known ASD genes.</p><h2>Other Information</h2><p dir="ltr">Published in: International Journal of Molecular Sciences<br>License: <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.3390/ijms241210394" target="_blank">https://dx.doi.org/10.3390/ijms241210394</a></p> |
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