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Metabolic mysteries: Three children with neurological symptoms and coagulopathy
Manage episode 400065585 series 3001064
Indhold leveret af JIMD Podcasts and Journal of Inherited Metabolic Disease. Alt podcastindhold inklusive episoder, grafik og podcastbeskrivelser uploades og leveres direkte af JIMD Podcasts and Journal of Inherited Metabolic Disease eller deres podcastplatformspartner. Hvis du mener, at nogen bruger dit ophavsretligt beskyttede værk uden din tilladelse, kan du følge processen beskrevet her https://da.player.fm/legal.
Shelby Mills on behalf of the UTH Medical Genetics Team, invites you to consider three mystery cases serving to hi-light some common, and some less common, presenting features for a treatable inherited metabolic disease. Arginase deficiency masked by cerebral palsy and coagulopathy—Three varied presentations of Latin American origin Shelby L. Mills, et al https://doi.org/10.1002/jmd2.12397
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