Search results
Results from the WOW.Com Content Network
In a motor vehicle accident, the vehicle jerks the neck forward and backward resulting in cervical spine damage. This is called whiplash. [17] The neurological and biological symptoms resulting from neck trauma emerge as a culmination of clinically isolated or combined symptoms caused by cervicocranial syndrome. [16]
Malan syndrome is defined by initial overgrowth and mild-to-severe intellectual disability. Almost all individuals with Malan syndrome display above-average height, weight, and head circumference in early life, but only one-third of adults with Malan syndrome are >2 standard deviations above the mean.
Among these measurements, the Autism Diagnostic Interview-Revised (ADI-R) and the Autism Diagnostic Observation Schedule (ADOS) are considered the "gold standards" for assessing autistic children. [ 24 ] [ 25 ] The ADI-R is a semi-structured parent interview that probes for symptoms of autism by evaluating a child's current behavior and ...
The ICD-10 equivalents also became part of its definition of autism spectrum disorder, as of the ICD-11. PDD-NOS included atypical autism, a diagnosis defined in the ICD-10 for the case that the criteria for autistic disorder were not met because of late age of onset, or atypical symptomatology, or both of these. [5] Even though PDD-NOS was ...
Classic autism, also known as childhood autism, autistic disorder, or Kanner's syndrome, is a formerly diagnosed neurodevelopmental disorder first described by Leo Kanner in 1943. It is characterized by atypical and impaired development in social interaction and communication as well as restricted, repetitive behaviors, activities, and interests.
There is ongoing current research into treatments that may improve some features of the condition. In 2020, a Phase 2A clinical trial by researchers at the Seaver Autism Center at Mount Sinai Hospital suggests that low-dose ketamine may be effective in treating clinical symptoms in children diagnosed with ADNP syndrome. [13] [14]
The syndrome typically results in intellectual disability, including motor and language delays. [2] [3] [4] Some individuals have had agenesis of the corpus callosum or aplasia of the cerebellar vermis. [1] [2] [3] This can sometimes manifest with symptoms of autism spectrum disorder. [2] [3] [4] Low muscle tone and strabismus are also common.
Rett syndrome is a neurodevelopmental disorder caused by a genetic mutation. [5] It occurs almost exclusively in girls. [5] A child with Rett syndrome experiences a loss of previously had intentional hand skills, and can experience a loss of language skills. [5] Children can also experience a loss of social skills and autism-like symptoms. [5]