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Clinical criteria for diagnosing autism inadequate for people with genetic conditions: Study


Clinical criteria for diagnosing autism inadequate for people with genetic conditions: Study
ANI |
Updated: Jan 02, 2021 09:05 IST
Cardiff [Wales], January 2 (ANI): The findings of a novel study suggests that more than half of individuals with one of four genetic conditions had significant autistic symptoms, despite not qualifying for a formal diagnosis.
People with certain genetic conditions are likely to have significant symptoms of autism, even if they do not meet all diagnostic criteria, the study concludes. Researchers at Cardiff University say their findings show clinical services need to adapt so that people diagnosed with autism-linked genetic conditions are not denied access to vital support and interventions. ....

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Study: Clinical criteria for autism diagnosis inadequate for individuals with genetic conditions


Study: Clinical criteria for autism diagnosis inadequate for individuals with genetic conditions
ANI |
Updated: Jan 02, 2021 05:56 IST
Washington [US], January 2 (ANI): A new research has discovered that people with certain genetic conditions are likely to have significant symptoms of autism, despite them not qualifying by formal diagnosis.
Published in The American Journal of Psychiatry, the international study analysed data from 547 people who had been diagnosed with one of four genetic conditions, also known as copy number variants (CNVs), associated with a high chance of autism - 22q11.2 deletion, 22q11.2 duplication, 16p11.2 deletion and 16p11.2 duplication.
Researchers at Cardiff University say their findings show clinical services need to adapt so that people diagnosed with autism-linked genetic conditions are not denied access to vital support and interventions. ....

United States , Helen Hyde , Tracy Elliot , Samuel Chawner , Head Of Research , Centre For Neuropsychiatric Genetics , Cardiff University , Cardiff University Copy Number Variant , Researchers At Cardiff University , American Journal , Neuropsychiatric Genetics , Diagnostic Interview Revised , Developmental Verbal Dyspraxia , Copy Number Variant , ஒன்றுபட்டது மாநிலங்களில் , ஹெலன் ஹைட் , தலை ஆஃப் ஆராய்ச்சி , மையம் க்கு நரம்பியல் மனநல ஜெநெடிக்ஸ் , கார்டிஃப் பல்கலைக்கழகம் , கார்டிஃப் பல்கலைக்கழகம் நகல் எண் மாறுபாடு , ஆராய்ச்சியாளர்கள் இல் கார்டிஃப் பல்கலைக்கழகம் , அமெரிக்கன் இதழ் , நரம்பியல் மனநல ஜெநெடிக்ஸ் , நகல் எண் மாறுபாடு ,