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pth 246 peds review Test

Enter the letter for the matching Answer
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1.
baby at full rounded while sitting A.4 mo B.5 mo C.1 mo D.2 mo
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2.
This deletion of Chromosome 15, will show failure to thrive for the infant, moderate MR, and hypotonia A.Cystic Fibrosis B.Cri-du-chat syndrome C.osteogenisis imperfecta D.Prader-Willi
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3.
a medicaid funded clinic where children w/ disabilities are seen, resources for equipment and medical needs available A.DDSN B.WIC C.CRS D.IDEA
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4.
progressive low tone and weakness, child may have a normal cognitive ability. Targets degeneration of the anterior horn of the spinal cord A.Cystic Fibrosis B.Becker's Muscular Dystrophy C.Arthrogryphosis Multiplex Congenita D.Spinal Muscular Atrophy
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5.
a law ensuring services to children w/ disabilities throughout the nation. Governs how states and pulic agencies provide early intervention? A.DDSN B.IDEA C.CRS D.IEP
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6.
This X linked condition causes a Neurodegenerative disorder, is more prominent in girls may wring hands A.Down syndrome B.Cerebral Palsy C.Angelman's syndrome D.Rhett Syndrome
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7.
age based on gross motor activities a child is able to do? A.chronological age B.adaptive age C.developmental age D.rounded age
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8.
what reaction orients head in space, may use visual / or gravity cues and occurs in the midbrain? A. labyrinthine B. Moro C. Primitive D. righting
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9.
a plan set by school officials with teachers, therapists and parent concerning specific goals and accomodations for a child A.IDEA B.CRS C.DDSN D.IEP
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10.
This boney defect will show a protrusion of the dura without the spinal cord A.Spina Bifida Occulta B.Spina Bifida Cystica C.Myelomeningocele D.Menginocele
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11.
This rare disease may be caused from intrauterine movement restrictions, hyperthermia in-utero. A.Prader-Willi syndrome B.Cri-du-chat C.Down syndrome D.Arthrogryphosis Multiplex Congenita
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12.
what are the 4 developmental time periods in everyone's life?
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13.
X-linked boys only, will show the Gower Maneuver, Dx:bone biopsy, death ~ 25 years A.Phynylkentonuria B.Becker's Muscular Dystrophy C.Fragile X Syndrome D.Duchenne Muscular Dystrophy
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14.
AVN of the femoral head seen in children 3-12, may have episodes of synovitis, may result in Trendelenburg gait, with interventions such as WB restrictions and aquatics. A.Osteogenisis imperfecta B.Rhett Syndrome C.LCPD D.Becker Muscular Distrophy
A.
LCPD
B.
righting
C.
Rhett Syndrome
D.
Duchenne Muscular Dystrophy
E.
Prader-Willi
F.
CRS
G.
Spinal Muscular Atrophy
H.
Arthrogryposis Multiplex Congenita
I.
infant, Childhood, adolescense, adulthood
J.
1
K.
IDEA
L.
IEP
M.
Meningocele
N.
developmental age
Type the Answer that corresponds to the displayed Question.
incorrect
15.
Findings of this syndrome will have a high tolerance to pain, 40-80% scholiosis, and an unusual skill with jigsaw puzzles. A.Prader-Willi B.ARthrogryposis Multiplex Congenita C.Prader-Willi D.Myelomeningocele
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16.
Normal gestation is A.36-37 weeks B.36-40 weeks C.37-42 weeks D.38-41 weeks
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17.
a paralysis of a C5-C6 showing s/sx of arm paresis hand rotated inward and failed MORO reflex on involved side. Prognosis is generally good A.Fetal alcohol syndrome B.TMH C.Erb's D.Bell's
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18.
This defect of Chromosome 7 leads to a pt with severe endurance problems. interventions may include inc UE str, chest PT. A.Chronic SMA B.Becker Muscular Dystorphy C.Duchenne Muscular Dystrophy D.Cystic Fibrosis
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19.
This trisomy 21 will show a babies 1/2 with heart defects and visual defects, ear infections and 10% severe MR A.Cri-du-chat B.Angelman's syndrome C.Down-syndrome D.Arthrogryposis Multiplex Congenita
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20.
This boney defect leaves an opening without a protrusion of the dura A.Meningocele B.Myelomenginocele C.Spina Bifida Cystica D.Spina Bifida Occulta
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21.
This type of SMA is onset at 2-17 years, has proximal weakness and slow progression A.Werdnig-Hoffman B.Acute infantile SMA C.Kugelburg-Welander D.Fragile X syndrome
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22.
This describes the way a child w/ Duchenee Muscular Dystrophy might use to go from laying to standing A.Adaptive positioning B.Asymmetrical standing C.Gower's manuver D.transition
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23.
A genetic cause of MR, with seizures, behavioral problems, may detect with a blood test, by be exacerbated by ingesting a chemical found in some gum and diet drinks
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24.
This gene defect occurs when one parent is affected by the gene Ex:osteogenesis imperfecta A.Dominant inheritance B.recessive inheritance C.sex-linked inheritance D.trisomies

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