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...

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Detalles Bibliográficos
Autores principales: Kowalik, Agnieszka, Gajewska, Danuta, Sykut-Cegielska, Jolanta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2018
Materias:
Original Article/Praca Oryginalna
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

Internet

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

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