Diagnosis is based on behavior, not cause or mechanism. Autism is defined in the DSM-IV-TR as exhibiting at least six symptoms total, including at least two symptoms of qualitative impairment in social interaction, at least one symptom of qualitative impairment in communication, and at least one symptom of restricted and repetitive behavior. Sample symptoms include lack of social or emotional reciprocity, stereotyped and repetitive use of language or idiosyncratic language, and persistent preoccupation with parts of objects. Onset must be prior to age three years, with delays or abnormal functioning in either social interaction, language as used in social communication, or symbolic or imaginative play. The disturbance must not be better accounted for by Rett syndrome or childhood disintegrative disorder.[77] ICD-10 uses essentially the same definition.[8] Several diagnostic instruments are available. Two are commonly used in autism research: the Autism Diagnostic Interview-Revised (ADI-R) is a semistructured parent interview, and the Autism Diagnostic Observation Schedule (ADOS) uses observation and interaction with the child. The Childhood Autism Rating Scale (CARS) is used widely in clinical environments to assess severity of autism based on observation of children.[21] A pediatrician commonly performs a preliminary investigation by taking developmental history and physically examining the child. If warranted, diagnosis and evaluations are conducted with help from ASD specialists, observing and assessing cognitive, communication, family, and other factors using standardized tools, and taking into account any associated medical conditions. A differential diagnosis for ASD at this stage might also consider mental retardation, hearing impairment, and a specific language impairment[78] such as Landau-Kleffner syndrome.[79] ASD can sometimes be diagnosed by age 14 months, although diagnosis becomes increasingly stable over the first three years of life: for example, a one-year-old who meets diagnostic criteria for ASD is less likely than a three-year-old to continue to do so a few years later.[19] In the UK the National Autism Plan for Children recommends at most 30 weeks from first concern to completed diagnosis and assessment, though few cases are handled that quickly in practice.[78] A 2006 U.S. study found the average age of first evaluation by a qualified professional was 48 months and of formal ASD diagnosis was 61 months, reflecting an average 13-month delay, all far above recommendations.[80] Clinical genetics evaluations are often done once ASD is diagnosed, particularly when other symptoms already suggest a genetic cause.[81] Although genetic technology allows clinical geneticists to link an estimated 40% of cases to genetic causes,[82] consensus guidelines in the U.S. and UK are limited to high-resolution chromosome and fragile X testing.[81] As new genetic tests are developed several ethical, legal, and social issues will emerge. Commercial availability of tests may precede adequate understanding of how to use test results, given the complexity of autism's genetics.[75] Metabolic and neuroimaging tests are sometimes helpful, but are not routine.[81] Underdiagnosis and overdiagnosis are problems in marginal cases, and much of the recent increase in the number of reported ASD cases is likely due to changes in diagnostic practices. The increasing popularity of drug treatment options and the expansion of benefits has given providers incentives to diagnose ASD, resulting in some overdiagnosis of children with uncertain symptoms. Conversely, the cost of screening and diagnosis and the challenge of obtaining payment can inhibit or delay diagnosis.[83] It is particularly hard to diagnose autism among the visually impaired, partly because some of its diagnostic criteria depend on vision, and partly because autistic symptoms overlap with those of common blindness syndromes.[84] The symptoms of autism and ASD begin early in childhood but are occasionally missed. Adults may seek retrospective diagnoses to help them or their friends and family understand themselves, to help their employers make adjustments, or in some locations to claim disability living allowances or other benefits.
Check out out wikipedia or http://www.autism-world.com/
No - autism is a neurological condition so it cannot show in a blood test, the only way to diagnose autism is with intensive assessment with a trained professional.
It comes down to a simple urine test. The chemical bufotenin makes up most of the autistic individual and is easy to detect. If it is not found within the urine, then the person must have some other obscure disorder.
No one 'gets' autism, it isn't s disease or an illness, autism is a difference like skin colour or sex - autism is a neurological difference, it is something that starts during the second trimester of pregnancy when the brain is forming. Issac Newton has a retrospective diagnosis - there is no test for autism, diagnosis is made by observing behaviour, specialists looked at the behaviour of Newton to determine that he could have been autistic.
no Added: Fragile X is like autism in that the condition can be a spectrum disorder, no or mild symptoms to severe symptoms. Fragile X is Genetic, the genetics of Autism are still being determined. Fragile X can be diagnosed any where by any doctor by a simple blood test, Autism is a subjective diagnosis based on evaluations and observations.
There are many different types of psychological tests that are done on children when testing them for autism. One of the more common ones is a behavioral assessment.
No, fortunately there is no pre-natal screening for autism.Some organisations, such as Autism Speaks, are aiming to bring about pre-natal screening in an attempt to stop Autistic people being born. As it is we don't know fully the causes of autism to be able to detect it outside of diagnosis from behaviour.
No, not yet. There is research investigating fetal testosterone levels via amniocentesis that might indicate a higher chance of autism, but that is based on the speculation that brains of people with autism are extreme male brains.
autism
Infantile Autism is when a baby or toddler (an Infant) has autism.
Autism is diagnosed by observation of the known characteristics in a person; there are several checklists and simple activities that can be used to aid this diagnosis either way. However, direct testing of an individual cannot define whether a person has autism or an autistic spectrum disorder, only whether it is not likely, likely or very likely that they do. This is because scientists are still not sure exactly what can and can't cause autism or ASD, and accordingly can't test for something whenthey don't know what to look for.
Biologial. Autism is neurodevelopmental. There are hereditary and genetic ties to autism.
No, Jedward do not have autism.