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Neurodevelopmental disorders
Diagnosed first in infancy, childhood or adolescence.
Developmental psychopathology
Study of how disorders arise and change with time.
disruption of early skills can affect later development.
Childhood-onset fluency disorder
Often call stuttering
is a communication and motor disorder
occurs twice as often in boys as girls
Language disorder
Limited speech in ALL situations
is a communication and motor disorder
occurs in 10 to 15% of children younger than 3 years of age.
Social (pragmatic) communication disorder
Difficulties with social aspects of verbal and nonverbal communication.
is a communication and motor disorder
Tourette’s disorder
Motor and vocal tics.
is a communication and motor disorder
high comorbidity with ADHD and OCD.
Attention Deficit/ Hyperactivity disorder
Central features of inattention, overactivity and impulsivity.
associated wiht behavioral, cognitive, social and academic impairments.
occurs in about 5% of children in the world.
general population 5 to 9%
Girls are less likely to be diagnosed.
symptoms appear around age 3 to 4
Specific learning disorders
Academic problems in reading, matematics and/or writing.
problems persist for six or more months despite targeted intervention.
5 to 15% prevalence.
reading difficulties are most common (7%)
Autism Spectrum Disorder
Includes what used to be called autisitc disorder, Asperger’s disorder, childhood disintegrative disorder and Rett Disorder.
problems in language, socialization and cognition.
pervasive
three levels of severity based on the amount of support needed.
Intellectual Disability (Intellectual Development Disorder)
Below average intellectual and adaptive functioning.
first evident in childhood
range of impairment varies greatly
IQ typically below 70 to 75.
prevalence of 1 to 3% of general population
chronic course
Lesch-Nyhan Syndrome
Intellectual disability, symptoms of cerebral palsy, self-injurious behaviors.
Phenylketonuria
Cannot break down phenylalanine which is found in some foods.
results in intellectual disability when the individual eats phenylalanine.
Down Syndrome
Most common chromosomal cause of intellectual disability
extra 21st chromosome.
distinctive physical symptoms.
Fragile X syndrome
Caused by mutation in the FMR1 gene on the X chromosome.
learning disabilities, hyperactivity, short attention span, gaze avoidance, persverative speech.
primarily affects males.
Cultural-Familial Intellectual Disability
Refers to intellectual disability influences by social and environmental factors such as:
abuse
neglect
social deprivation