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On Trunk Orthoses

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OPZ250 Mesleki Yabancı Dil I

14

.hafta

Reference Review And Discussion

On Trunk Orthoses

&

Multiple Sclerosis

Prof. Dr.Serap Alsancak

Doç. Dr. Senem Güner

Dr. Öğr. Gör. Enver Güven

Öğr. Gör. Ali Reza Vasefmia

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Multiple Sclerosis

Glendaliz Bosques MD ■ _David W. Pruitt MD

Description

Autoimmune progressive demyelinating disease of the central nervous system (CNS), which is prevalent in adults but uncommon in children.

Etiology/Types

■ _Relapsing-remitting (most common) ■ _Primary progressive

■ _Secondary progressive ■ _Progressive-relapsing Risk Factors

■ _Environmental factors (viral exposure, country of origin, sun exposure, and temperate climate) may play a role

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Clinical Features

■ _Polyfocal or polysymptomatic neurologic deficits

■ _Isolated optic neuritis (higher risk of developing MS if bilateral) ■ _Isolated brain-stem dysfunction

■ _Isolated dysfunction of the long tracts

■ _Fatigue (severe enough to limit school performance or recreational activities)

■ _Encephalopathic signs (usually absent in adults) such as headaches, vomiting, seizures, and altered mental status

■ _Bladder dysfunction (urgency and frequency more frequent than obstructive symptoms) ■ _Heat sensitivity (Uhthoff’s phenomenon) causes exacerbation or worsening of symptoms with increased body temperature

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Natural History

■ _Involvement of CNS white matter leads to clinical neurological impairments. Remission usually follows. Other episodes involve different areas of the white matter

■ _Episodes are spread over time (at least two distinct neurologic episodes) and location (evidence of lesions seen by clinical findings, magnetic resonance imaging (MRI), computed tomography, or evoked potentials)

■ _Time to recover from clinical exacerbation is shorter in children (4.3 weeks vs up to 8 weeks in adults)

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Diagnosis

Differential diagnosis ■ _CNS infection ■ _CNS malignancy

■ _Primary small-vessel vasculitis of the CNS ■ _Macrophage-activation syndrome

■ _Inherited white matter leukodystrophies ■ _Transverse myelitis

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History

More than one clinical episode of the following occurs: ■ _Muscular weakness

■ _Sensory deficits

■ _Visual disturbances: blurry vision, partial blindness, and diplopia ■ _Coordination deficits

■ _Bulbar impairments

■ _Dysautonomia: vertigo, headaches, somnolence, tinnitus, and sphincter incompetence

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