Congenital insensitivity to pain associated with PRDM12 mutation: Two case reports and a literature review

Background: PRDM12 is a newly discovered gene responsible for congenital insensitivity to pain (CIP). Its clinical manifestations are various and not widely known. Methods: The clinical data of two infants diagnosed with CIP associated with PRDM12 mutation were collected. A literature review was per...

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Detalles Bibliográficos
Autores principales: Yu, Hanrui, Wu, Jie, Cong, Jinju, Chen, Mingxiong, Huang, Yifei, Yu, Jifeng, Wang, Liqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067717/
https://www.ncbi.nlm.nih.gov/pubmed/37021010
http://dx.doi.org/10.3389/fgene.2023.1139161

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067717/
https://www.ncbi.nlm.nih.gov/pubmed/37021010
http://dx.doi.org/10.3389/fgene.2023.1139161

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