Congenital Insensitivity To Pain With Anhidrosis
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
- 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
- Congenital insensitivity to pain with anhidrosis
From NCATS Genetic and Rare Diseases Information Center
- Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.
Rotthier Annelies, et al. Brain : a journal of neurology 2009 10 (Pt 10) 2699-711
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- Page last reviewed:Feb 1, 2023
- Page last updated:May 30, 2023
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