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Pediatric-onset multiple sclerosis in Egypt: a multi-center registry of 186 patients

Authors :
Hamdy,Sherif
Abdel-Naseer,Maged
Shalaby,Nevin
Elmazny,Alaa
Girgis,Marian
Nada,Mona
Hassan,Amr
Mourad,Husam
Hegazy,Mohamed
Abdelalim,Ahmed
Kishk,Nirmeen
Abokrysha,Noha
Genedy,Shaimaa
Essawy,Ehab
Shehata,Hatem
Hamdy,Sherif
Abdel-Naseer,Maged
Shalaby,Nevin
Elmazny,Alaa
Girgis,Marian
Nada,Mona
Hassan,Amr
Mourad,Husam
Hegazy,Mohamed
Abdelalim,Ahmed
Kishk,Nirmeen
Abokrysha,Noha
Genedy,Shaimaa
Essawy,Ehab
Shehata,Hatem
Publication Year :
2018

Abstract

Sherif M Hamdy,1 Maged Abdel-Naseer,1 Nevin M Shalaby,1 Alaa Elmazny,1 Marian Girgis,2 Mona A Nada,1 Amr Hassan,1 Husam S Mourad,1 Mohamed I Hegazy,1 Ahmed Abdelalim,1 Nirmeen A Kishk,1 Noha T Abokrysha,1 Shaimaa A Genedy,1 Ehab A Essawy,3 Hatem S Shehata1 1Neurology Department, Cairo University, Cairo, Egypt; 2Pediatric Department, Cairo University, Cairo, Egypt; 3Division of Biochemistry, Chemistry Department, Faculty of Science, Helwan University, Helwan, Egypt Introduction: Although the frequency of pediatric-onset multiple sclerosis (POMS) has increased in recent decades, it is still highly uncommon, which creates a need for the involvement of more registries from various clinical centers.Objective: To characterize the demographic, clinical, and paraclinical features of Egyptian patients with POMS.Patients and methods: A retrospective chart review study was undertaken on 237 Egyptian patients with demyelinating events which started before the age of 18 years who attended one of five tertiary referral centers in Cairo, Egypt.Results: Multiple sclerosis was diagnosed in 186 patients, 47 (25.27%) patients had disease onset before the age of 12 years; “early-onset pediatric multiple sclerosis (EOPMS)”. The mean age of disease onset was (14.13±2.49 years), with a female:male ratio of 1.62:1, none of the enrolled patients had a primary progressive course (PPMS), whereas 10 patients (5.38%) had a secondary progressive form. Approximately two-thirds of the patients had monofocal disease onset, and less than 10% presented with encephalopathy; most of them had EOPMS. Motor weakness was the presenting symptom in half of the patients, whereas cerebellar presentation was detected in 34.95%, mainly in EOPMS. Seizures (not related to encephalopathy) were more frequent in those with EOPMS. Initial brain magnetic resonance images were positive in all patients, with detected atypical lesions in 29.03%, enhanced lesions in 35.48%, black hol

Details

Database :
OAIster
Notes :
text/html, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1024288823
Document Type :
Electronic Resource