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Subarachnoid Block a Safe Choice for Cesarean Section in Neurofibromatosis Patient with Severe Kyphoscoliosis

Neurofibromatosis type 1 (NF1) is an autosomal-dominant neuroectodermal hereditary disorder, in which spinal skeletal deformities are one of the manifestations. Pectus carinatum, temporomandibular joint dysfunction, and kyphoscoliosis can be seen with this genetic disorder which can lead to cardiore...

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Detalles Bibliográficos
Autores principales:	Demir, Ibrahim, Kılıç, Ebru Tarıkçı, Akdemir, Mehmet Salim
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2018
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872880/ https://www.ncbi.nlm.nih.gov/pubmed/29628596 http://dx.doi.org/10.4103/aer.AER_222_17

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