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29 Cards in this Set

  • Front
  • Back
femlaes ever manifest the condition?
x-linked recessive
Duchenne muscular dystrophy age typically notice
2 to 5 years of age
characteristics of 2 to 5 years of age with ducheen muscular dystropny
difficulty, running, walking, climbing stairs, and toe walking
Gower's sign
stand-up from sitting on the floor, hands to push up on his knees and thighs to set into full standing position
characteristics age ranges 5-10
IQ 80 to gifted
characteristics 10-12
loss ability to walk and scolosis
teenage and beyond
need power wheelchair, assitance eating, 50% have cardiomyopathy- die late teens or early 20s
Denmark respriatory treatment
Mechanical ventilation, have a great quality of life and adapted vans, housing, and other supports are available
Gene therapy in treatment of muscular dystrophy
one the horizon; clone dystophine protein (large gene); myoblast transplanatation
5 accomodations
wheelchair accessible desk, locate proper position in the classroom, reposition chair, have resource room near emergency exit, rest breaks and lie down, shortened day
Life span expectations
Type I- early infancy to 2 years

Type II- normal lifespan
survive preschool years congnitive function
normal
function productively in the regualr classroom
yes
etiology of CF
autosomal recessive genetic disease; both parents have to be carries; 25% have, 25% totoally affected, 50% carrier, genetic disorder of chromosome 7
carrier rate of CF in the U.S.
7 milliom to 10 million
2 carriers marrying and having children
fairly high- carrier 1 in 30 adults
common characteristics of cystic fibrosis
99% of infants with meconiumileus have DG, fatty deposits appear in stool; foul order (undigested fats), frequent gas
CF typcially diagnosised
the 1st and 2nd of birth or infancy or early childhood
sweat test
stimulating a small area of the skin (forearm) to sweat by a small electric current and medication; 40meq/k- infants and >3 months 60meq/k
vest clearance system; how used to treat CF
clear the airway; inflatasble vest worn 20 to 30 mins.
planning to live vs. planning to die
Planning to live to enjoy school, family life, and adulthood
degenerative conditions
reminder dependent on medical support, different, viligent
longevity predictions
understand the disease, follow medical regimens, and comm. with medical personnel, cope with feelings of grief, fear, and loss
Elizabeth Kubler-Ross
Denial, anger, barganing, and acceptance
Home teaching and
type of normalcy and distraction form their disease
Maintaing Academic Focus
discipline, fatigue- montior carefully, disscuss death
learned helpnesses
Experience elevated depression and reduced self-esteem; inapprorately relies on others and displays reduced intitaite for everyday tasks
Maintaing Academic Focus
discipline, fatigue- montior carefully, disscuss death
learned helpnesses
Experience elevated depression and reduced self-esteem; inapprorately relies on others and displays reduced intitaite for everyday tasks