Common Pediatric Disorders Flashcards

1
Q

What is OBPI?

A

Injury of BS during delivery (traction and rotation during delivery)
Most common at C5-C6 (Erb’s Palsy)
-Other version (C7-T1) = Klumpke’s Palsy

Complete UE paralysis possible but unlikely
-Check for fracture of clavicle and humerus.

RARELY BILATERAL!!!!!!!!!!!!!!!!!!!!

Treat early; prognosis is good with treatment

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2
Q

What is Hydrocephalous?

A

Water in the brain

  • Increased production
  • Decreased absorption
  • Decreased flow (obstruction)

Common cause = subarachnoid hemorrhage
Obstructive causes = ductal stenosis and brain tumor

May or may not be associated with increased intracranial pressure

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3
Q

Symptoms in Hydrocephalous?

A
Wide head
Downward eyes (Setting Sun)
-Spasticity, Clonus, brisk reflexes
\+Babinski
-Lethargy, mood changes, papilledema, etc

Treat with VP shunt

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4
Q

Flow of CSF?

A

Per Rijo:

CSF Flow

  1. lateral ventricles
  2. interventricular formamina
  3. 3rd ventricle
  4. cerebral aqueduct
  5. 4th ventricle
  6. subarachnoid space
  7. returns to venous system via arachnoid granulations
  8. most of the CSF empty into the superior sagittal sinus
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5
Q

Know what an MRI of Hydrocephalus looks like

A

LVs look huge

Diagnosed in newborns with ultrasound
(For children, CT and MRI are used. And fundoscopic eye exam)

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6
Q

Risks and mechanisms for shunting

A

VP Shunt: blocked easily, high risk for infection.
Some develop aggressive behaviors
If VP Shunt is dysfunctional, there may be an acute onset of hydrocephalus

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7
Q

Myelodysplasia Occulta?

A

Not visible - defect of vertebral body; no protrusion of spinal cord

No treatment!

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8
Q

Myelodysplasia (Aperta) - Myelocele

A

Protrusion of spinal cord at the back with no cystic meningeal covering

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9
Q

Myelodysplasia (Aperta) - Myelomeningocele

A

Protrusion of spinal cord and meninges through back - cystic

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10
Q

Myelodysplasia (Aperta) - Meningocele

A

Bulging of meninges through back without presence of spinal cord, usually well-covered with skin (may also protrude anteriorly into abd)

  • ** All 4 use MRI for diagnosis (after birth; prenatal = US)
  • 3 Apertas can use CT w/ contrast too
  • –Treated with surgery and PT after
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11
Q

Arnold Chiari?

A

Downward displacement of cerebellar tonsils through foramen magnum - sometimes causing non-communicating hydrocephalus as a result of obstruction of CSF outflow

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12
Q

Clinical manifestations of Down Syndrome?

A
Widen nasal bridge
Low set ears
Single palmar crease
Wide-spaced 1st toe
Hypotonia
Pelvic dysplasia
Mental retardation
Cardiac malformations (AV canal)
Ligamentous laxity (AAI)
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13
Q

Diagnosis and Prognosis of DS?

A

Diagnosis:

  • Prenatal: Serum for MSAFL, US, Aminocentesis at 15-20 wks GA, Chorionic villus sampling at 11-12 weks GA
  • Post-natal: Karotype, Cardiac evaluation, Thyroid function

Treatment: Management is most services for development. Radiographs NOT RECOMMENDED for cervical instability

Prognosis: depends on:

  • Level of mental retardation
  • Access to services
  • Good muscular training for stability
  • Presence of co-morbidities
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14
Q

What is CP?

A

Group of motor syndromes resulting from disorders of early brain development (4 types). Commonly caused by early brain injury from infection, ischemia, endocrine/genetic disorders, prematurity, asphyxia, kernicterus

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15
Q

Is UE or LE affected more in hemiplegic CP?

A

UE

-Growth arrest of one arm or hand is common

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16
Q

What is seen in Spastic Diplegia?

A

Severe adduction of hips, dragging of legs while crawling, brisk reflexes, +Babinski, ankle clonus, Equinovarus (walks on tip-toes, if walking). Normal intellect common

Best prognosis of all 4.

17
Q

Characteristic of Sapstic Quadriplegia?

A

Swallowing difficult
Mos severe
MOST OFTEN ASSOCIATED WITH MENTAL RETARDATION AND SEIZURES!
Flexion contractures of knees and elbows

18
Q

Athetoid (Dyskinetic CP)

A
Hypotonia!! (others show spansticity)
Poor head control
Feeding and speech dysfunctions
UMN dysfunction and seziures uncommon
Intellect usually preserved

Ataxia, writing movements, etc.