EPISODE · Feb 9, 2024 · 5 MIN
Metabolic mysteries: Three children with neurological symptoms and coagulopathy
from JIMD Podcasts · host Journal of Inherited Metabolic Disease
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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Metabolic mysteries: Three children with neurological symptoms and coagulopathy
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