Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical disease

Galactosemia is an inborn error of galactose metabolism caused by mutations in the GALT gene. Though early detection and galactose restriction prevent severe liver disease, affected individuals have persistently elevated biomarkers and often neuro-developmental symptoms. We present a teenage compoun...

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Detalles Bibliográficos
Autores principales: Cocanougher, Benjamin, Aypar, Umut, McDonald, Amber, Hasadsri, Linda, Bennett, Michael J., Edward Highsmith, W., D'Aco, Kristin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471153/
https://www.ncbi.nlm.nih.gov/pubmed/28649529
http://dx.doi.org/10.1016/j.ymgmr.2014.12.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471153/
https://www.ncbi.nlm.nih.gov/pubmed/28649529
http://dx.doi.org/10.1016/j.ymgmr.2014.12.004

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