Congenital methemoglobinemia type II in a 5‐year‐old boy

Congenital Methemoglobinemia is a rare neurologic condition which can mimic other diseases such as epilepsy syndromes and leukodystrophies. The responsible gene, CYB5R3, is not typically included on commonly order neurologic and epilepsy panels. We recommend that laboratories include this gene on th...

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Detalles Bibliográficos
Autores principales: Mannino, Elizabeth A., Pluim, Thomas, Wessler, Jacob, Cho, Megan T., Juusola, Jane, Schrier Vergano, Samantha A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771927/
https://www.ncbi.nlm.nih.gov/pubmed/29375859
http://dx.doi.org/10.1002/ccr3.1310

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771927/
https://www.ncbi.nlm.nih.gov/pubmed/29375859
http://dx.doi.org/10.1002/ccr3.1310

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