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Genes (Basel) ; 12(11)2021 10 22.
Article in English | MEDLINE | ID: mdl-34828273

ABSTRACT

Novel genome editing and transient gene therapies have been developed the past ten years, resulting in the first in-human clinical trials for monogenic disorders. Syndromic autism spectrum disorders can be caused by mutations in a single gene. Given the monogenic aspect and severity of syndromic ASD, it is an ideal candidate for gene therapies. Here, we selected 11 monogenic ASD syndromes, validated by animal models, and reviewed current gene therapies for each syndrome. Given the wide variety and novelty of some forms of gene therapy, the best possible option must be decided based on the gene and mutation.


Subject(s)
Autism Spectrum Disorder/therapy , Genetic Therapy , Animals , Autism Spectrum Disorder/genetics , CRISPR-Cas Systems , Gene Editing/methods , Genetic Therapy/methods , Genetic Therapy/trends , Humans , Mutation
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