Congenital Anomalities Flashcards

1
Q

injections of Dextrose (a regenerative irritant into the ligaments or joints
that Stimulates the Release growth factors and collagen deposits
Increases ligament and tendon size
Repairs articular cartilage defects

A

vertebral block treatment

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2
Q

how do you treat hemivertebrae

A

Surgical excision early in childhood
In an adult with a hemivertebra in the lower lumbar spine
OMT –
Used to keep spine mobile prior to surgery creating better outcome
To help body adapt to heel lift

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3
Q

anomaly most found in lumbar spine, T11, T12, T1 and may be associated with kyphoscoliosis

A

butterfly vertebra

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4
Q

Buttock dimpling, “Sitting Buddah”,
Extended knees, flexed hips and equinovarus feet
Treatment: Operative, Spinal stabilization for progressive kyphosis & scoliosis
Limb amputation

A

Sacral Agenesis

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5
Q

since L1-2 facets are more sagittal ot limits

A

rotation

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6
Q

since L4-5 facets are more coronal it limits

A

flexion

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7
Q

Disc herniation signs and symptoms

A

Antalgic gait, lean toward the side of the disc herniation, pain sciatic sharp shooting pain radiation from buttock to posterior thigh to calf and into the foot
Pain with prolong sitting increases
Straight leg raising test positive with pain to the back
Weakness in big toe dorsiflexion with numbness

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8
Q

whats different between iliolumbar ligament and facet pain

A

Iliolumbar ligament pain = low back, hip and groin area
Facet pain = local pain/pressure at affected joint and the hip, buttock & back of thigh with extension,

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9
Q

’ fracture in the pars interarticularis of the vertebral arch

A

spondylolysis

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10
Q

Incomplete closure of the pars (L5-S1)
Posterior facet joints
Elongation of the pars interarticularis
Pars remains intact

A

congenital spondylolisthesis

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11
Q

Clinical Presentation in Young people < 30 years: dysplastic spondylolisthesis

A

Brought in for evaluation for change in gait or posture, Gait = stiff legged, short stride, waddling, Tight hamstrings working to stabilize the L5-S1 junction

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12
Q

isthmic spondylolisthesis

A

most common type. Caused by repetitive stress fractures to the pars interarticularis, especially due to hyperextension. Pars stress fracture occurs around 5-7 years of age, t common at L5-S1 (Cumulative stress)

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13
Q

Spondylisthesis type A,B,C

A

Dysplastic Type:
Pars defect at L5—S1 has horizontal facet allowing entire vertebra with posterior elements to slip forward
Creating drop off sign between L5-S1
Isthmic Type:
Pars defect at L5-S1 allows anterior vertebral body to slip forward leaving the posterior elements. Drop off felt at L4-L5
Degenerative:
L4-L5 has no pars defect but degenerative facets and disc
Drop off sign felt between L4-L5

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14
Q

Sacralization

A

One or both of the L5 transverse processes either:
Articulates with a pseudoarthrosis (Batwing Transverse Process)
Fuses with the sacrum (Partial at L5)

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15
Q

Lumbarization

A

Lumbarization: Failure of S1 to fuse with the rest of the Sacrum (less common)

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16
Q

What can cause spina bifida

A

Inadequate Folate intake
Use of folic acid antagonists (methotrexate)
Genetic factors causing abnormal folate metabolism
Antiepileptic drugs (Valproate; Carbamazepine)
Diabetes (maternal)
Amniotic bands; disrupt neural tube development

17
Q

Tethered Cord: Indications for Surgery

A

Progressive neurological deterioration in terms of motor, sensory or urinary dysfunction in a child

18
Q

Occurs when the spinal cord is abnormally attached to surrounding tissue

A

tethered cord

19
Q

Occurs just after primary neurulation with defects in the mesodermal cells in the somites which migrate medially to surround the neural tube to form vertebrae, posterior spinal arches, meninges, and paraspinous muscles
Notochordal remnants remain as the nucleus pulposus of the intervertebral disc

A

Closed Spinal Dysraphism (Spina Bifida Occulta)

20
Q

over lumbosacral spine associates with congenital anomalies including spinal dysraphism Two Types: segmental lesions & span the midline
Most often associated with tethered cord and lipomeningocele

A

hemangioma