Os odontoideum in wolcott-rallison syndrome: a case series of 4 patients

Wolcott-Rallison Syndrome is the commonest cause of neonatal diabetes in consanguineous families. It is associated with liver dysfunction, epiphyseal dysplasia, and developmental delay. It is caused by mutations in eukaryotic translation initiation factor 2-α kinase 3 (EIF2AK3). We report 4 children...

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Detalles Bibliográficos
Autores principales: Dias, R. P., Buchanan, C. R., Thomas, N., Lim, S., Solanki, G., Connor, SEJ, Barrett, T. G., Kapoor, R. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748609/
https://www.ncbi.nlm.nih.gov/pubmed/26860746
http://dx.doi.org/10.1186/s13023-016-0397-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748609/
https://www.ncbi.nlm.nih.gov/pubmed/26860746
http://dx.doi.org/10.1186/s13023-016-0397-z

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