| Literature DB >> 32124676 |
Omar Abdel-Mannan1, Rosa Cortese2, Evangeline Wassmer3, Cheryl Hemingway4, Alan Thompson5, Wallace Brownlee2, Olga Ciccarelli6, Yael Hacohen1.
Abstract
Previous cohort studies on paediatric multiple sclerosis (MS) have reported very low frequencies for a primary progressive MS (PPMS) course ranging from 0% to 7%. We identified six patients presenting prior to the age of 18 years and fulfilling the 2017 McDonald Criteria for PPMS. Presentation with progressive neurological symptoms and signs in young people should prompt evaluation for genetic causes such as leukodystrophies, hereditary spastic paraparesis and mitochondrial diseases given the rarity of primary progressive course in paediatric MS. In the absence of an alternative diagnosis, with new therapeutic options becoming available for PPMS, this diagnosis should then be considered.Entities:
Keywords: MS mimics; McDonald criteria; Primary progressive multiple sclerosis; disease modifying therapies; paediatric multiple sclerosis
Mesh:
Year: 2020 PMID: 32124676 DOI: 10.1177/1352458520910361
Source DB: PubMed Journal: Mult Scler ISSN: 1352-4585 Impact factor: 6.312