Congenital Insensitivity to Pain due to a de novo L369P mutation in the SCN11A gene with Heterotrophic Ossification - A Case Report

INTRODUCTION: A male child with congenital insensitivity to pain (CIP) due to a novel de novo L369P mutation in the SCN11A gene was found to have significant bilateral hip flexion contractures, followed by severe heterotopic ossification after contraction release. This is the first report to describ...

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Detalles Bibliográficos
Autores principales: Makar, Gabriel, Kahlon, Sundeep, Seeley, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465737/
https://www.ncbi.nlm.nih.gov/pubmed/37654749
http://dx.doi.org/10.13107/jocr.2023.v13.i08.3798

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465737/
https://www.ncbi.nlm.nih.gov/pubmed/37654749
http://dx.doi.org/10.13107/jocr.2023.v13.i08.3798

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