![]() Your child or another family member has syndromic ASD.Genetic testing is more likely to find a genetic cause for ASD if Most people with syndromic ASD have a genetic cause for their ASD. Some people with ASD have syndromic ASD, meaning that they have other specific features in addition to having ASD, such as looking different from other people in the family or having birth defects. Genetic testing looks for causes of ASD but cannot be used to diagnose ASD. If your child is diagnosed with ASD, the doctor might refer your child for genetic counseling and testing. Genetic testing and autism spectrum disorder If you are pregnant or planning a pregnancy, your doctor might recommend carrier screening if you have a family health history of a genetic disorder, such as fragile X syndrome. Learn how early intervention leads to better outcomes for children with ASD. Also, a diagnosis of ASD is important for tailoring children’s education once they start school. ![]() If a child is diagnosed at a young age with ASD, treatment is more effective. A reliable diagnosis of ASD is more common around 2 or 3 years of age and usually made by a developmental specialist. When a child is closely monitored, signs of ASD can sometimes be noticed at 18 months or younger. The doctor may check your child more closely for early signs of ASD and might refer your child to a specialist for further evaluation. Knowing about your family health history of ASD can help your child’s doctor better care for your child. What might the doctor recommend for your child if you have a family health history of autism spectrum disorder? Consider including older family members who have or had signs of ASD, even if they were not diagnosed with ASD, as ASD diagnoses were less common in the past and might have been missed.īe sure to share your family health history of ASD with your child’s doctor and other family members.Be sure to include anyone who received a diagnosis that is no longer used, such as Asperger syndrome or mental retardation and. ![]()
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