Ophthalmic findings of congenital insensitivity to pain with anhidrosis with a novel neurotrophic tyrosine kinase receptor type 1 gene mutation: A case report

We report a case of congenital insensitivity to pain with anhidrosis (CIPA) with a novel neurotrophic tyrosine kinase receptor type 1 (NTRK1) gene mutation. The patient suffered from recurrent corneal ulcer. A slit-lamp examination revealed ciliary hyperemia, bulbar conjunctival edema, epithelial de...

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Detalles Bibliográficos
Autores principales: Zhu, Rong, Zhu, Yuxiang, Xu, Mingpeng, Gu, Zhensheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489851/
https://www.ncbi.nlm.nih.gov/pubmed/36160132
http://dx.doi.org/10.3389/fmed.2022.955929

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489851/
https://www.ncbi.nlm.nih.gov/pubmed/36160132
http://dx.doi.org/10.3389/fmed.2022.955929

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