Congenital Insensitivity To Pain
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Last Posted: Mar 05, 2023
- Congenital insensitivity to pain with anhidrosis syndrome: A series from Jordan.
Masri Amira, et al. Clinical neurology and neurosurgery 2019 0 105636 - Heterogeneity of clinical features and mutation analysis of NTRK1 in Han Chinese patients with congenital insensitivity to pain with anhidrosis.
Li Ningbo, et al. Journal of pain research 2019 0 453-465 - Molecular genetic analysis in 21 Chinese families with congenital insensitivity to pain with or without anhidrosis.
Zhao F, et al. European journal of neurology 2020 0 (8) 1697-1705 - Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohort.
Cintra Vivian Pedigone, et al. Journal of the neurological sciences 2021 0 117498 - Intrafamilial Phenotypic Variability Associated with the I1739V Mutation in the SCN9A Gene.
Peddareddygari Leema Reddy, et al. Case reports in neurology 2022 0 (1) 135-139 - Two novel mutant alleles of the gene encoding neurotrophic tyrosine kinase receptor type 1 (NTRK1) in a patient with congenital insensitivity to pain with anhidrosis: a splice junction mutation in intron 5 and cluster of four mutations in exon 15.
Bodzioch M, et al. Human mutation 2001 0 (1) 72 - Associations between single-nucleotide polymorphisms in the NTRK1 gene and basal pain sensitivity in young Han Chinese women.
Li Ningbo, et al. Neuroscience letters 2017 10 - Phenotypes and Genotypes in Five Children with Congenital Insensitivity to Pain with Anhidrosis.
Wang Qing-Li, et al. Pediatric neurology 2016 4 - The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility.
Holliday Kate L, et al. Molecular pain 2012 0 (1) 72 - Congenital insensitivity to pain
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- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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