Quiz 2 (congenital disorders, pediatric sport injuries/ limp deficiency) Flashcards

1
Q

Multiple congenital joint contractures in the first trimester fetal development

A

ARTHROGRYPOSIS MULTIPLEX CONGENITA

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2
Q

ARTHROGRYPOSIS MULTIPLEX CONGENITA Sign and symptoms in the mother.

A

Maternal fevers, infection, vascular compromise, limited room in the uterus, low amts of amniotic fluid

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3
Q

what are the most affected parts of ARTHROGRYPOSIS MULTIPLEX CONGENITA

A

hands, wrists, elbows, ankles, knees and hips.

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4
Q

Signs and symptoms of ARTHROGRYPOSIS MULTIPLEX CONGENITA in babies

A

Joint contractures, dislocations, decreased muscle strength, dislocations, diminished reflexes and Diminished skin creases

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5
Q

what are interventions for ARTHROGRYPOSIS MULTIPLEX CONGENITA

A

Stretching and strengthening to gain and sustain ROM and inc. strength.
Elbow ROM imperative for Independence in ADLs; core, hip, knee strength vital for postural control

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6
Q

Abnormality of chromosome 21: can be trisomy, translocation, or mosaicism.

A

DOWN SYNDROME

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7
Q

Clinical Signs and symptoms for DOWN SYNDROME

A

Hypotonia, short stature, upward slant of eyes, small ears, single transverse palmar crease, cognitive limitation.
May include cardiac defects, duodenal atresia, atlantoaxial instability, thyroid defects, hearing loss, epicanthal folds

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8
Q

What are family edu, for down syndrome parents

A

guidelines to incorporate handling, positioning, and developmental skills.

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9
Q

What does physical therapy focus on for downs syndrome

A

Focus on function and independence: improving coordination skills, and developmental skills; stability of joints and cocontraction

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10
Q

what are indications for a SMO (Sure step supramalleolar orthotic)

A
Pronation
Hypotonia
Triplanar instability in weight bearing
Inability to stand independently
Mild toe-walking
Developmental delay
Delay in acquiring gross motor skills
Poor coordination or balance
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11
Q

Contraindications that and SMO might not be the right fit

A
High muscle tone
Spasticity
Severe toe-walking
Tight heel cords
Tight peroneals
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12
Q

Incomplete closure of spinal column

A

SPINA BIFIDA

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13
Q

Generally affects the neuromuscular and genitourinary systems.

A

SPINA BIFIDA

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14
Q

most benign no neuromuscular or genitourinary involvement

A

Spina bifida occulta

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15
Q

Spinal cord begins to protrude

A

Meningocele-meninges

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16
Q

flaccid LEs, loss of sensation below the defect, often seen in L-S area

A

Meningocele-meninges

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17
Q

Warning signs of a shunt malfunction

A

irritability, personality changes, increased sleepiness, downward gaze, headaches.

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18
Q

The cerebellum, pons, and medulla may protrude into the foramen magnum

A

Hydrocephalus as result of Arnold-Chiari defect.

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19
Q

Clinical Signs and symptoms of Arnold-Chiari defect

A

Bowel and bladder dysfunction (catheterization)

Latex allergies

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20
Q

Clinical Signs and symptoms of Tethered cord syndrome

A

spinal cord fixed caudally: dec. strength, inc. spasticity in LEs, changing uro sx, back pain, scoliosis

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21
Q

What are comorbidities c meningomyelocele

A

skin breakdown, vasomotor changes, soft tissue contractures, cognitive and social delays

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22
Q

What does physical therapy focus on for spina bifida

A

Active stretching and strengthening, inc. endurance for mobility, developing independent tx skills.

Seating and positioning
Supported standing
Provision of orthotics,

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23
Q

What is the goal for children c spina bifida

A

independence in functional skills

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24
Q

Recognized as a neurobiological disorder….May also have ADD, ADHD, anxiety, deafness, depression, obsessive compulsive disorder, Tourette Syndrome

A

AUTISM

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25
Clinical signs and symptoms of Autism
Poor eye contact Flat affect; unable to interpret facial or gestural cues from others Prefer aloneness Reciprocal behaviors such as sharing are difficult Delay in language skills development Unable or unmotivated to engage in conversation.
26
CLINICAL SIGNS-Onset prior to age 3 of autism
May perseverate on a word or phrase Intense interest in narrow area of interest Adhere to rituals Stereotypical motor behaviors: rocking and flapping of the hands Very sensitive to sound, touch, bright lights, odors High tolerance for pain
27
Genetic condition with abnormality on X chromosome Hand wringing Head growth slows Often severe difficulty with walking and trunk movements
Rett syndrome
28
Above average or average IQ Deficiencies in social skills Difficulties with transitions or changes Obsessive routines
ASPERGER SYNDROME
29
When does AUTISM become evident
Begin appearing 12-18 months; almost always evident between 24 months and 6 yea
30
occurs when a bone bends and cracks, instead of breaking completely into separate pieces
Greenstick fracture
31
when are incidences for sport injuries greater for children
Intense, repetitive training during periods of growth
32
When can a child begin strength training
When child can follow instructions on proper technique.
33
How is strength gained c children
Strength gain is due to improved coordination and neuromuscular recruitment
34
What is recommended when doing strength training c children
Recommended is low weight high rep for adolescents
35
Differences between adults and children bones
Child: bone is more porous and susceptible to compression fractures
36
Salter-Harris Fracture Classification
identifies where in the growth plate the fx occurs
37
Where are growth plate fx more commonly found
found near joints; where injuries commonly occur(weakest area around joints)
38
what can growth plate injuries lead to
can lead to alternation in normal bone growth
39
Osteochondritis dessicans
is an injury to the articular cartilage
40
Common sites of growth plate fx
Elbow, knee and ankle
41
what are the most common fx of the foot
Stress fx
42
What are the physical difference of children from adults
Smaller heart size Decreased stroke volume Decreased volume of blood Strength gains are more indicative of neuromuscular gains in coordination and recruitment of muscles than in pure strength as in adult
43
Most common of all spine injuries
lumbar spine injuries
44
Fracture with no vertebral movement is a
spondylolysis
45
if the vertebra translates anteriorly.
Spondylolisthesis
46
Common sites of lumbar injuries
L4-5 and L5-S1.
47
One of the most common shoulder injuries
proximal humeral growth plate fracture.
48
what is the usual cause proximal humeral growth plate fracture.
underdeveloped musculature of the shoulder
49
Clavicular fx usually cause
a fall to the lateral aspect of the shoulder.
50
Little league elbow pain around
Medial epicondyle
51
Avulsion fx occur
site of muscle attachment sites
52
treatment at the site of an avulsion
stretching
53
results of a quick and abrupt muscle contraction
avulsion fx
54
A slipped capital femoral epiphysis can result from
trauma or overuse
55
most common site for overuse injury in children
Knee
56
is an avulsion of the bone where the patellar tendon attaches to the bone of the tibia.
Osgood Schlatter disease
57
Treatment for Osgood Schlatter’s disease
Ice for pain and inflammation Aggressive stretching program Exercise with emphasis on eccentric ex
58
Patellar pain syndrome treatment
Strengthening of VMO: Stretching of the TFL and the iliotibial band.
59
Malalignment between the patella and distal femur.
Patellar pain syndrome
60
VMO may be weak allowing excess motion of the patella on the femur.
Patellar pain syndrome
61
Excess genu valgus
Patellar pain syndrome
62
Inflammation between posterior tibialis and soleus and the periosteum of the tibia. Excessive pronation is a common cause
Shin splints-Medial tibial stress syndrome
63
Sx is medial tibial pain
Shin splints-Medial tibial stress syndrome
64
Shin splints treatment
Corrections of gait deficiencies during walking and running. Landing more toward midfoot than the heel Aquatic ex, stretching and strengthening
65
Interventions for amputees
Shape and desensitize residual limb Plan a program of exercise for strengthening Improve endurance Improve tolerance for wear of prosthetic
66
occur in utero; common cause is amniotic band syndrome
Congenital
67
entire bone missing
Amelia
68
all or part of one bone is missing
Hemiamelia
69
?-trauma, tumors, infections, or burns | 2x more common than the congenital
Acquired-trauma,
70
proximal bone is missing
phocomelia-