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  2. Jan 6, 2018 · Autism spectrum disorder has no single known cause. Given the complexity of the disorder, and the fact that symptoms and severity vary, there are probably many causes. Both genetics and environment may play a role. Genetics. Several different genes appear to be involved in autism spectrum disorder.

  3. Aug 20, 2019 · Genetic modifiers in autism spectrum disorder. Autism is estimated to be 40–80% heritable. However, both genetic and non-genetic factors modulate the penetrance of risk genes, resulting in a highly heterogeneous disease phenotype for similar pathogenic variants. Examples of genetic modulators include CNV, epigenetics, and double-hit mutations.

    • Lauren Rylaarsdam, Alicia Guemez-Gamboa
    • 10.3389/fncel.2019.00385
    • 2019
    • Front Cell Neurosci. 2019; 13: 385.
  4. Aug 20, 2021 · The etiology of ASD is likely to be multifactorial, with both genetic and non-genetic factors playing a role . ASD can be syndromic or non-syndromic. Syndromic ASD is often associated with chromosomal abnormalities or monogenic alterations. Such examples include Rett syndrome, fragile X syndrome, and MECP2 duplication syndrome . Contrary to ...

    • Ann Katrin Sauer, Janelle E. Stanton, Sakshi Hans, Andreas M. Grabrucker
    • 2021
  5. Mar 31, 2021 · Autism is complex, and no two autistic people are the same. Because of this, researchers believe there are probably many causes of autism, including genetic and environmental factors.

  6. May 28, 2021 · But less than 1 percent of non-syndromic cases of autism stem from mutations in any single gene. So far, at least, there is no such thing as an ‘ autism gene ’ — meaning that no gene is consistently mutated in every person with autism. There also does not seem to be any gene that causes autism every time it is mutated.

  7. The specific causes of autism spectrum disorder are not fully understood, although they are often related to genetic factors. For parents of one child with ASD, risk of having another child with ASD is around 3 to 10%. Several genetic abnormalities, such as Fragile X syndrome, tuberous sclerosis complex, and Down syndrome, may be associated ...

  8. Feb 26, 2021 · The clinical heterogeneity of autism is mirrored by a complex genetic architecture involving several types of common and rare variants, ranging from point mutations to large copy number variants, and either inherited or spontaneous ( de novo ).

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