Motor and functional evaluation of patients with spastic paraplegia, optic atrophy, and neuropathy (SPOAN) Avaliação motora e funcional de pacientes com paraplegia espástica, atrofia óptica e neuropatia (SPOAN)
Spastic paraplegia, optic atrophy, and neuropathy (SPOAN) is an autosomal recessive complicated form of hereditary spastic paraplegia, which is clinically defined by congenital optic atrophy, infancy-onset progressive spastic paraplegia and peripheral neuropathy. In this study, which included 61 ind...
Main Authors: | Zodja Graciani, Silvana Santos, Lucia Inês Macedo-Souza, Carlos Bandeira de Mello Monteiro, Maria Isabel Veras, Simone Amorim, Mayana Zatz, Fernando Kok |
---|---|
Format: | Article |
Language: | English |
Published: |
Academia Brasileira de Neurologia (ABNEURO)
2010-02-01
|
Series: | Arquivos de Neuro-Psiquiatria |
Subjects: | |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2010000100002 |
Similar Items
-
Clinical features and management of hereditary spastic paraplegia
by: Ingrid Faber, et al.
Published: (2014-03-01) -
Translation and validation into Brazilian Portuguese of the Spastic Paraplegia Rating Scale (SPRS)
by: Katiane R. Servelhere, et al.
Published: (2016-06-01) -
Motor impairment in a rare form of spastic paraplegia (Spoan syndrome): a 10-year follow-up
by: Cláudia R. C. Galvão, et al.
Published: (2019-10-01) -
Hereditary spastic paraplegia from 1880 to 2017: an historical review
by: Ingrid Faber, et al. -
PHYSIOTHERAPEUTIC INTERVENTION IN PATIENTS AFFECTED BY THE SYNDROME OF SPOAN: AN EXPERIENCE REPORT
by: Neila Alves de Queiroz, et al.
Published: (2019-07-01)