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pth 246 peds review
review on peds
| Question | Answer |
|---|---|
| baby at full rounded while sitting A.4 mo B.5 mo C.1 mo D.2 mo | 1 |
| 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 | righting |
| what are the 4 developmental time periods in everyone's life? | infant, Childhood, adolescense, adulthood |
| age based on gross motor activities a child is able to do? A.chronological age B.adaptive age C.developmental age D.rounded age | developmental age |
| 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 | IEP |
| 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 | CRS |
| 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 | IDEA |
| 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 | Erb's |
| 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 | LCPD |
| 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 | Duchenne Muscular Dystrophy |
| 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 | Phenylkentonuria |
| 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 | Spinal Muscular Atrophy |
| 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 | Kugelburg-Welander SMA |
| 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 | Cystic Fibrosis |
| 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 | Gower's manuver |
| 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 | Arthrogryposis Multiplex Congenita |
| 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 | Prader-Willi |
| 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 | Prader-Willi |
| This boney defect leaves an opening without a protrusion of the dura A.Meningocele B.Myelomenginocele C.Spina Bifida Cystica D.Spina Bifida Occulta | Spina Bifida Occulta |
| Normal gestation is A.36-37 weeks B.36-40 weeks C.37-42 weeks D.38-41 weeks | 37-42 weeks |
| 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 | Rhett Syndrome |
| 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 | Meningocele |
| 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 | dominant inheritance |
| 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 | Down-syndrome |
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