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Corrigendum to “Brown-Vialetto-Van Laere syndrome and Fazio-Londe syndrome: A novel mutation and in silico analyses” [J. Clin. Neurosci. 72 (2020) 342–349]

Published:August 10, 2022DOI:https://doi.org/10.1016/j.jocn.2022.07.026
      The authors would like to inform the readers that the correct affiliation of Dr. Mohammad Kazem Bakhshandeh is given above. The authors would like to apologise for any inconvenience caused.

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      • Brown-Vialetto-Van Laere syndrome and Fazio-Londe syndrome: A novel mutation and in silico analyses
        Journal of Clinical NeuroscienceVol. 72
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          Brown-Vialetto-Van Laere syndrome (BVVLS; 211530) has a very low frequency in the world. A few cases has been reported yet worldwide. Its features mostly include bulbar palsy, progressive sensorineural hearing loss (SNHL), hypotonia and respiratory compromises varying from infancy ages to adulthood ages) [3]. Additional features may include swallowing difficulty, facial diplegia, progressive muscle impairment, absence of gag reflex, decreased diaphragm motility and premature death. If not treated, affected individuals die at 9 months − 42 years [3].
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