J Neurol Sci. 2015 Jun 19. pii: S0022-510X(15)00375-5. doi: 10.1016/j.jns.2015.06.034. [Epub ahead of print]
Author information
- 1Department of Neurology, Federal University of the State of Rio de Janeiro-UNIRIO, Brazil; Department of Neurology, Hospital da Lagoa, Ministry of Health, Rio de Janeiro, Brazil.
- 2Department of Neurology, Federal University of the State of Rio de Janeiro-UNIRIO, Brazil. Electronic address: fercostapereira@yahoo.com.br.
- 3Department of Neurology, Federal University of the State of Rio de Janeiro-UNIRIO, Brazil.
Abstract
OBJECTIVE:
To describe familial forms of demyelinating diseases from an MS referral center in Río de Janeiro State, Brazil.
METHODS:
A descriptive, cross-sectional study was done to identify familial IIDD cases in Hospital da Lagoa, a public hospital where 75% of patients with IIDD who live in Rio de Janeiro state, located in the Southeast region of Brazil, are referred. The diagnoses of all consecutive patients followed in 2011 were reviewed to apply new diagnostic criteria (Wingerchuk et al., 2008). The diagnosis of IIDD was confirmed based on clinical history, neurological examination, MRI of the skull and spinal cord, CSF analysis and investigation of IgG NMO antibodies. The cases that had at least one other relative with IIDD were selected for the study.
RESULTS:
Familial forms were found only in the multiple sclerosis (MS) and neuromyelitis optica syndrome (NMOSD) categories. 23 MS families were identified, 60.86% with first degree kinship. It has a Caucasian preponderance, 90% of whom were white. The frequency of early onset was 15% and 20% of the MSf cases have progressive primary course.
CONCLUSION:
The frequency of familial cases of IIDD was 6.12% among MS patients and 2.8% in NMO spectrum syndromes.
Copyright © 2015. Published by Elsevier B.V.