4.6 Article

Demographics and ocular findings in children with myasthenia

Journal

EYE
Volume 37, Issue 4, Pages 700-704

Publisher

SPRINGERNATURE
DOI: 10.1038/s41433-022-02030-5

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This study retrospectively analyzed the medical records of pediatric patients with myasthenia gravis who were examined at Great Ormond Street Hospital between 2016 and 2020. The study found that juvenile myasthenia gravis, particularly the ocular form, was the most common type of myasthenia gravis in children. Ptosis was the most common presenting sign, and the majority of patients showed improvement after medical treatment.
Purpose To report the demographics and ocular features of myasthenia gravis in the paediatric population. Methods Retrospective revision of the medical records of all patients younger than 18 years of age with myasthenia who were examined at Great Ormond Street Hospital between the 1st of January 2016 and 1st of January 2020. Results A total of 49 children were assessed during the 4-year period. There was a female predominance, with only 12 males (24.5%). 26 children (53.1%) had juvenile myasthenia gravis (JMG) while 18 (36.7%) had congenital myasthenic syndrome (CMS). 4 patients (8.2%) were diagnosed with probable CMS while 1 (2.0%) was classified as probable JMG. The mean age at diagnosis was 5.3 years old (SD 3.9) whereas the mean age at onset was 3.7 years old (SD 3.9). Almost half of the children (49%) had ocular involvement, present in 19 patients in the JMG group (70.4%) and in 5 children (22.7%) in the CMS cohort. Ptosis was the most common sign at presentation, seen in 32 patients (65.3%). Nine patients (18.4%) presented with a squint and another 7 (14.3%) developed it later on. Anti-acetylcholine receptor antibodies were positive in 18 of the 26 JMG patients (69.2%) whereas identifiable mutations were found in the 18 CMS patients (100%). Pyridostigmine was the drug of choice in our series, used by thirty-three patients (67.3%). The majority of the patients (73.5%) improved after treatment. Conclusions JMG was the most common type of paediatric MG, specifically the ocular form. Ptosis was the most common sign at presentation. The majority of the patients improved after medical treatment.

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