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- W1990384219 abstract "Fazio Londe Syndrome is a rare neurological disorder presenting with progressive bulbar palsy with respiratory failure. Initially considered to have an unrelenting course, is now found to be due to mutations in the SLC52A3 gene which encodes the intestinal (hRFT2) riboflavin transporter in some children. We report an 11-year-old child with features of Fazio Londe syndrome who presented to our Institute with respiratory failure." @default.
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- W1990384219 date "2014-01-01" @default.
- W1990384219 modified "2023-09-27" @default.
- W1990384219 title "Fazio Londe syndrome: A treatable disorder" @default.
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- W1990384219 doi "https://doi.org/10.4103/0972-2327.144283" @default.
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