1. ONSET OF THIS DISEASE
IS CHARACTERIZED IN EARLY ADULT LIFE. THERE OCCURS PROFUSE NEUROLOGICAL
DISTURBANCES WITH REGULAR PERIODS OF FLUCTUATIONS, EXACERBATION AND IMPROVEMENT.
THE CAUSE IS UNKNOWN BUT VARIOUS THEORIES ABOUT DEGENERATIVE, TOXIC AND
DEFICIENCY STATES HAVE BEEN FORWARDED.
3.
SYMPTOMS OF THE DISEASE ARE
SUDDEN
MOTOR AND SENSORY DISTURBANCES, | |
DIFFUSED
NEUROLOGICAL SIGNS, | |
CLUMSINESS, | |
IMPAIRED
SENSATIONS, | |
EXTREME
WEAKNESS, | |
STAGGERING
GAIT, | |
LOWER
LIMBS WHICH ARE USUALLY AFFECTED, FEEL HEAVY AND WOODEN |
4.
THE MAIN CAUSE IS DESTRUCTION OF MYLIN, A LIPID SUBSTANCE, WHICH PROTECTS
THE NERVE FIBER AND IS ESSENTIAL FOR PROPER CONDUCTION OF IMPULSES.
5. The
initial attack AND SUBSEQUENT RELAPSES OCCUR AFTER ACUTE
INFECTIONS
NUMBNESS
OF EXTREMITIES, ATAXIA, VISUAL DISTURBANCES | |
SPASTIC
PARALYSIS | |
DEEP
TENDON REFLEXES ARE INCREASED | |
BILATERAL
EXTENSOR PLANTER RESPONSE | |
NYSTAGMUS | |
WEAKNESS | |
THE
WIDESPREAD NEUROLOGICAL LESIONS CAN NOT BE EXPLAINED BY ANYONE ANATOMIC
BASIS. |
7.
THESE SIGNS AND SYMPTOMS ARE SUBJECT TO ACUTE EXACERBATION AND
REMISSIONS. THESE TWO CHARACTERISTICS MAKE EARLY DIAGNOSIS VERY DIFFICULT
8.
LABORATORY FINDINGS ARE—
GAMMA GLOBULIN ARE INCREASED IN CEREBROSPINAL FLUID, OLIGOCLONAL BANDS OF IgC MAY SOME TIMES BE DETECTED IN
ELECTROPHORESIS OF CEREBROSPINAL FLUID VISUAL EVOKED POTENTIAL TO BOTH FLASH AND
PATTERN ARE ABNORMAL, WITHOUT KNOWN SIGNS OR HISTORY OF VISUAL IMPAIRMENT. MRI
SCAN OF HEAD OR /AND SPINAL CORD MAY SHOW LESIONS.
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Last modified: February 17, 2001