Uniparental isodisomy of chromosome 1 results in glycogen storage disease type III with profound growth retardation

BACKGROUND: Glycogen storage disease type III (GSDIII) is caused by mutations of AGL gene with debranching enzyme deficiency. Patients with GSDIII manifest fasting hypoglycemia, hepatomegaly, hepatopathy, myopathy, and cardiomyopathy. We report on an 18‐year‐old boy with a profound growth retardatio...

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Detalles Bibliográficos
Autores principales: Ponzi, Emanuela, Alesi, Viola, Lepri, Francesca R., Genovese, Silvia, Loddo, Sara, Mucciolo, Mafalda, Novelli, Antonio, Dionisi‐Vici, Carlo, Maiorana, Arianna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503021/
https://www.ncbi.nlm.nih.gov/pubmed/30916492
http://dx.doi.org/10.1002/mgg3.634

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503021/
https://www.ncbi.nlm.nih.gov/pubmed/30916492
http://dx.doi.org/10.1002/mgg3.634

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