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 |