Literature DB >> 16829007

Subacute sclerosing panencephalitis: is there something different in the younger children?

Deniz Yilmaz1, Omer Faruk Aydin, Nesrin Senbil, Deniz Yuksel.   

Abstract

Subacute sclerosing panencephalitis is a rare, slow viral infection caused by a defective measles virus. Although it is a rare disease, it is still important in developing countries. The onset is generally between the ages of 5-15 years. We reported the clinical and laboratory profile and nature of 9 patients under the age of 4 years with SSPE. Although it is known that a few patients with SSPE have an acute and rapidly fulminating course, in this study rate of progression was rapidly progressive in 6 patients and progressive in 3 of them on admission. Unfortunately, 4 of them were lost to follow up because of address and/or telephone number alterations. Although the number of patients in this study is not sufficient, we suggest that SSPE patients under the age of 4 years have a poor prognosis as a result of progressive or rapidly progressive course despite medical treatment.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16829007     DOI: 10.1016/j.braindev.2006.04.008

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  3 in total

Review 1.  Subacute sclerosing panencephalitis.

Authors:  Ravindra Kumar Garg
Journal:  J Neurol       Date:  2008-10-14       Impact factor: 4.849

2.  Genetic characterization of measles virus genotype D6 subacute sclerosing panencephalitis case, Alberta, Canada.

Authors:  K Pabbaraju; K Fonseca; S Wong; M W Koch; J T Joseph; G A Tipples; R Tellier
Journal:  J Neurovirol       Date:  2018-10-05       Impact factor: 2.643

3.  Seizures as onset symptoms and rapid course in preschool children with subacute sclerosing panencephalitis.

Authors:  Shuang Liao; Min Zhong; Nan Zou; Tingsong Li; Li Jiang
Journal:  Brain Behav       Date:  2021-02-05       Impact factor: 2.708

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.