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      Multiple sclerosis in childhood: clinical features of 149 cases.

      Multiple Sclerosis (Houndmills, Basingstoke, England)
      Adolescent, Age of Onset, Child, Disabled Persons, Disease Progression, Female, Humans, Male, Multiple Sclerosis, epidemiology, physiopathology, Recurrence, Retrospective Studies

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          Abstract

          From the retrospective study of 3375 patients affected by clinically definite or probable multiple sclerosis (MS), 149 patients were collected with onset of the disease before the age of 16 years (4.4%). Female/male ratio was higher than that of the adult onset MS (AOMS) population (2.2 vs 1.6) particularly at ages of onset after 12 years (3.0, P = 0.007 vs AOMS). Among initial symptoms, those suggesting brainstem dysfunction (25%) were more frequent compared to other systems and compared to AOMs symptoms; motor and sensory disturbances were slightly less frequent (respectively 17.5% and 18.3%). Optic neuritis appeared in 16.5% of cases with onset in childhood and in 16.2% of cases with AOMS, cerebellar disturbances respectively in 9.1% and 7.7%. The first interattack-interval and the clinical course of early onset MS did not differ significantly from AOMS. In early onset MS patients with disease duration < 8 years, cases with EDSS > 6 were slightly more frequent than in the AOMS group (P = 0.04). The frequency of cases for different levels of disability was similar for disease duration > 8 years.

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          Author and article information

          Journal
          9160345
          10.1177/135245859700300105

          Chemistry
          Adolescent,Age of Onset,Child,Disabled Persons,Disease Progression,Female,Humans,Male,Multiple Sclerosis,epidemiology,physiopathology,Recurrence,Retrospective Studies

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