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4 Cards in this Set
- Front
- Back
Distinguishing features |
3/3 persistent deficits in social communication/interaction and 2+/4 restricted, repetitive behavior, interests, or activities present in early developmental period Severity of social and behavior clusters (level of support) With/out accompanying intellectual impairment With/out accompanying language accompaniment Associated with a known medical or genetic condition or environmental disorder Associated with another neurodevelopmental, mental, or behavioral disorder With catatonia |
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Prevalence |
1% lifetime 3-4 times more prevalent in women than men Underdiagnosed in African Americans 15% associated with genetic mutation |
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Course and onset |
Onset: very early at 1-2 years old Delayed language often 1st along with odd sociality improvement likely, though only minority functioning independent with high impairment |
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Diagnostic Criteria |
A. Persistent deficits in social communication and social interaction across multiple contexts, as manifested by all of the following, currently or by history: 1. Deficits in social-emotional reciprocity, ranging, from abnormal social approach and failure of normal back-and-forth conversation; to reduced sharing of interests, emotions, or affect; to failure to initiate or respond to social interactions 2. Deficits in nonverbal communicative behaviors used for social interaction, ranging from poorly integrated verbal and nonverbal communication; to abnormalities in eye contact and body language or deficits in understanding and use of gestures; to a total lack of facial expressions and nonverbal communication 3. Deficits in developing, maintaining, and understanding relationships, ranging from difficulties adjusting behavior to suit various social contexts; to difficulties in sharing imaginative play or in making friends; to absence of interest in peers B. Restricted, repetitive patterns of behavior, interests, or activities as manifested by at least 2 of the following, currently or by history 1. Stereotyped or repetitive motor movements, use of objects, or speech (simple motor stereotypies, lining up toys or flipping objects, echolalia, idiosyncratic phrases) 2. Insistence on sameness, inflexible adherence to routines or ritualized patterns of verbal or nonverbal behavior (extreme distress at small changes, difficulties with transitions, rigid thinking patterns, greeting rituals, need to take same route or eat same food every day) 3. Highly restricted, fixated interests that are abnormal in intensity or focus ( strong attachment to or preoccupation with unusual objects, excessively circumscribed or preservative interests) 4. Hyper or hyporeactivity to sensory input or unusual interest in sensory aspects of the environment (apparent indifference to pain/temperature, adverse response to specific sounds or textures, excessive smelling or touching of objects, visual fascination with lights or movement) C. Symptoms must be present in the early developmental period (but may not fully manifest until social demands exceed limited capacities or may be masked by learned strategies in later life) D. Symptoms cause clinically significant impairment in areas of functioning E. Disturbances are not better explained by intellectual developmental disorder or global developmental delay. IDD and ASD frequently co-occur Specifiers Requiring very substantial support Requiring substantial support Requiring support With or without accompanying intellectual impairment With or without accompanying language impairment Associated with a known genetic or other medical condition or environmental factor Associated with a neurodevelopmental, mental, or behavioral problem With catatonia |