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Difficulties in The Dietary Management of a Girl with Two Diseases Requiring a Special Diet
3-Methylcrotonylglycinuria (3-MCG) is an autosomal recessive inborn error of leucine metabolism caused by the deficiency of 3-methylocrotonyl-CoA carboxylase (3-MCC deficiency). It is the most commonly detected organic aciduria in newborn screening conducted by tandem mass spectrometry (MS/MS) [1, 2...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Sciendo
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522887/ https://www.ncbi.nlm.nih.gov/pubmed/30281517 http://dx.doi.org/10.34763/devperiodmed.20182203.225228 |