Catastrophic results due to unrecognizing of congenital insensitivity to pain with anhidrosis in children with multiple long bones fractures: A case report of 27 years follow-up of two siblings

INTRODUCTION: Congenital insensitivity to pain with anhidrosis (CIPA; OMIM 256,800) is a rare autosomal recessive disease. Although the clinical symptoms are known, the consensus of CIPA treatment has not been recognized. This is the first report of CIPA in Indonesia, a case of two siblings, male an...

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Detalles Bibliográficos
Autores principales: Hartono, Franky, Tanjung, Conny, E Besinga, Karina, Marpaung, Daniel, Ananditya, Tessi, Budisantoso, Andrew Budiartha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381489/
https://www.ncbi.nlm.nih.gov/pubmed/32707409
http://dx.doi.org/10.1016/j.ijscr.2020.07.010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381489/
https://www.ncbi.nlm.nih.gov/pubmed/32707409
http://dx.doi.org/10.1016/j.ijscr.2020.07.010

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