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A rare cause of congenital hypotonia and bulbar palsy: a case of brown-vialetto-van laere syndrome type 1 in infancy

: International Journal of Family & Community Medicine
: Wesley Alfredo Gawlinski de Arruda,¹ Daniela Rigo,² Lianna S Facco,³ Helen Luiza Silvestrini,⁴ Leandra de Oliveira Rigo⁵

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Keywords

brown-vialetto-van laere syndrome, congenital hypotonia, bulbar palsy, riboflavin, SLC52A3, case report

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