Impaired neural structure and function contributing to autonomic symptoms in congenital central hypoventilation syndrome

Congenital central hypoventilation syndrome (CCHS) patients show major autonomic alterations in addition to their better-known breathing deficiencies. The processes underlying CCHS, mutations in the PHOX2B gene, target autonomic neuronal development, with frame shift extent contributing to symptom s...

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Detalles Bibliográficos
Autores principales: Harper, Ronald M., Kumar, Rajesh, Macey, Paul M., Harper, Rebecca K., Ogren, Jennifer A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626648/
https://www.ncbi.nlm.nih.gov/pubmed/26578872
http://dx.doi.org/10.3389/fnins.2015.00415

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626648/
https://www.ncbi.nlm.nih.gov/pubmed/26578872
http://dx.doi.org/10.3389/fnins.2015.00415

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