Congenital Insensitivity To Pain: Fracturing Without Apparent Skeletal Pathobiology Caused By An Autosomal Dominant, Second Mutation in SCN11A Encoding Voltage-Gated Sodium Channel 1.9

Congenital insensitivity to pain (CIP) comprises the rare heritable disorders without peripheral neuropathy that feature inability to feel pain. Fracturing and joint destruction are common complications, but lack detailed studies of mineral and skeletal homeostasis and bone histology. In 2013, disco...

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Dettagli Bibliografici
Pubblicato in:Bone
Autori principali: Phatarakijnirund, Voraluck, Mumm, Steven, McAlister, William H., Novack, Deborah, Wenkert, Deborah, Clements, Karen L., Whyte, Michael P.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2015
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4755825/
https://ncbi.nlm.nih.gov/pubmed/26746779
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2015.11.022
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