Difficult intubation management in a child with I-cell disease

I-cell disease (mucolipidosis II) is a rare metabolic disorder resulting from the deficiency of a specific lysosomal enzyme, N-acetylglucosamine-1-phosphotransferease. Developmental delay and growth failure are common presentations of I-cell disease. Psychomotor deterioration is rapid and progressiv...

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Detalles Bibliográficos
Autores principales: M. Mahfouz, Abdul Kader, George, G., Al-Bahlani, Suhaila S., Al Nabhani, Mohamed Z.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945506/
https://www.ncbi.nlm.nih.gov/pubmed/20927271
http://dx.doi.org/10.4103/1658-354X.65121

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945506/
https://www.ncbi.nlm.nih.gov/pubmed/20927271
http://dx.doi.org/10.4103/1658-354X.65121

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