Disease | tic disorder |
Phenotype | C0004352|autism |
Sentences | 8 |
PubMedID- 22132206 | Children and adolescents with a history of co-morbid psychiatric or medical conditions (e.g., epilepsy), a history of head injury, or of a genetic disorder associated with autism (e.g., fragile x syndrome), were excluded. |
PubMedID- 22348382 | In that study, an extensive literature search was conducted looking for articles describing genetic disorders in patients with autism, asd, pervasive developmental disorder, asperger syndrome, or autistic/autistic-like traits/features/behavior, using pubmed and google scholar, as well as follow-up of references cited in the papers thus identified. |
PubMedID- 21858456 | While pws is one of several genetic disorders associated with autism, this co-occurrence is much less well-researched than autism in the context of fragile x, 22q deletion, tuberous sclerosis, rett, smith–lemi–optiz, or other genetic conditions (for reviews, see betancur 2011; grafodatskaya et al. |
PubMedID- 20858229 | The mtor pathway is dysregulated in several other genetic disorders that are associated with autism, such as tuberous sclerosis (ts) [57]. |
PubMedID- 21541322 | Adolescents with a co-morbid psychiatric or medical condition (e.g., epilepsy), history of head injury, or genetic disorders associated with autism (e.g., fragile x syndrome) were excluded. |
PubMedID- 24289166 | A total of 42 (8.8%) children had a known possible genetic or non-genetic risk factor for autism (39 children with autistic disorder, three children with pdd-nos; table 4). |
PubMedID- 25984535 | The present study demonstrates that while the prevalence of asd is similar in both arabs and jews, arabs were more commonly diagnosed with autistic disorder (including cases with severe autism who received a higher clinical cars score). |
PubMedID- 24198778 | These findings, together with the observation that many genetic disorders associated with autism often result in microcephaly (betancur, 2011), suggest that early increased brain growth is present in only a subset of individuals with asd (raznahan et al., 2013a). |
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