Inflammatory Demyelinating Central Nervous System Diseases in Childhood: Clinical and Paraclinical Profiles in 133 Patients

In a retrospective review of patients with acquired demyelinating disorders of the central nervous system, 133 patients (5.6%) whose diseases started in childhood, were selected from 2369 patients, who had medical records in the Neurology Department of Dokuz Eylul University. Out of 133, 98 had rela...

Full description

Bibliographic Details
Main Authors: Derya Kaya, Egemen İdiman, Serkan Özakbaş
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Autoimmune Diseases
Online Access:http://dx.doi.org/10.1155/2012/957802
id doaj-915d6c16a2ab4c2db71e5f961d64c3ae
record_format Article
spelling doaj-915d6c16a2ab4c2db71e5f961d64c3ae2020-11-25T00:56:29ZengHindawi LimitedAutoimmune Diseases2090-04222090-04302012-01-01201210.1155/2012/957802957802Inflammatory Demyelinating Central Nervous System Diseases in Childhood: Clinical and Paraclinical Profiles in 133 PatientsDerya Kaya0Egemen İdiman1Serkan Özakbaş2Department of Neurology, Ordu State Hospital, 52200 Ordu, TurkeyDepartment of Neurology, Faculty of Medicine, Dokuz Eylul University, 35340 Izmir, TurkeyDepartment of Neurology, Faculty of Medicine, Dokuz Eylul University, 35340 Izmir, TurkeyIn a retrospective review of patients with acquired demyelinating disorders of the central nervous system, 133 patients (5.6%) whose diseases started in childhood, were selected from 2369 patients, who had medical records in the Neurology Department of Dokuz Eylul University. Out of 133, 98 had relapsing remitting multiple sclerosis, 21 had secondary progressive multiple sclerosis, 8 had clinically isolated syndrome, 3 had neuromyelitis optica, 2 had Marburg disease, and 1 had radiologically isolated syndrome. In 55 patients (41.3%), disease onset was before age 16. Polysymptomatic presentation (22.6%) was the most common initial feature. The EDSS scores ranged from 0 to 9 with a median of 2.0 () for 126 patients. MRI records of 111 patients were obtained. 97 patients had clinically definite multiple sclerosis. 11 MS patients (11.3%) did not initially present the diagnostic MRI features. All of the remaining multiple sclerosis patients fulfilled Barkhof-Tintore criteria (100%) and 88.7% fulfilled KIDMUS criteria. Cranial MRI of NMO patients was normal. Our findings demonstrate some important clinical and paraclinical features that can help the literature on acquired demyelinating disorders of childhood by utilizing data from Western Turkey.http://dx.doi.org/10.1155/2012/957802
collection DOAJ
language English
format Article
sources DOAJ
author Derya Kaya
Egemen İdiman
Serkan Özakbaş
spellingShingle Derya Kaya
Egemen İdiman
Serkan Özakbaş
Inflammatory Demyelinating Central Nervous System Diseases in Childhood: Clinical and Paraclinical Profiles in 133 Patients
Autoimmune Diseases
author_facet Derya Kaya
Egemen İdiman
Serkan Özakbaş
author_sort Derya Kaya
title Inflammatory Demyelinating Central Nervous System Diseases in Childhood: Clinical and Paraclinical Profiles in 133 Patients
title_short Inflammatory Demyelinating Central Nervous System Diseases in Childhood: Clinical and Paraclinical Profiles in 133 Patients
title_full Inflammatory Demyelinating Central Nervous System Diseases in Childhood: Clinical and Paraclinical Profiles in 133 Patients
title_fullStr Inflammatory Demyelinating Central Nervous System Diseases in Childhood: Clinical and Paraclinical Profiles in 133 Patients
title_full_unstemmed Inflammatory Demyelinating Central Nervous System Diseases in Childhood: Clinical and Paraclinical Profiles in 133 Patients
title_sort inflammatory demyelinating central nervous system diseases in childhood: clinical and paraclinical profiles in 133 patients
publisher Hindawi Limited
series Autoimmune Diseases
issn 2090-0422
2090-0430
publishDate 2012-01-01
description In a retrospective review of patients with acquired demyelinating disorders of the central nervous system, 133 patients (5.6%) whose diseases started in childhood, were selected from 2369 patients, who had medical records in the Neurology Department of Dokuz Eylul University. Out of 133, 98 had relapsing remitting multiple sclerosis, 21 had secondary progressive multiple sclerosis, 8 had clinically isolated syndrome, 3 had neuromyelitis optica, 2 had Marburg disease, and 1 had radiologically isolated syndrome. In 55 patients (41.3%), disease onset was before age 16. Polysymptomatic presentation (22.6%) was the most common initial feature. The EDSS scores ranged from 0 to 9 with a median of 2.0 () for 126 patients. MRI records of 111 patients were obtained. 97 patients had clinically definite multiple sclerosis. 11 MS patients (11.3%) did not initially present the diagnostic MRI features. All of the remaining multiple sclerosis patients fulfilled Barkhof-Tintore criteria (100%) and 88.7% fulfilled KIDMUS criteria. Cranial MRI of NMO patients was normal. Our findings demonstrate some important clinical and paraclinical features that can help the literature on acquired demyelinating disorders of childhood by utilizing data from Western Turkey.
url http://dx.doi.org/10.1155/2012/957802
work_keys_str_mv AT deryakaya inflammatorydemyelinatingcentralnervoussystemdiseasesinchildhoodclinicalandparaclinicalprofilesin133patients
AT egemenidiman inflammatorydemyelinatingcentralnervoussystemdiseasesinchildhoodclinicalandparaclinicalprofilesin133patients
AT serkanozakbas inflammatorydemyelinatingcentralnervoussystemdiseasesinchildhoodclinicalandparaclinicalprofilesin133patients
_version_ 1725226951053934592