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

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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Bibliographic Details
Main Authors: Rong Zhu, Yuxiang Zhu, Mingpeng Xu, Zhensheng Gu
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-09-01
Series:Frontiers in Medicine
Subjects:
congenital insensitivity to pain with anhidrosis (CIPA)
NTRK1
cornea
neurotrophic keratopathy
dry eye
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2022.955929/full

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https://www.frontiersin.org/articles/10.3389/fmed.2022.955929/full

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