Neuromyotonia: associated disorders
Evidence-based neurology checklist on neuromyotonia: associated disorders: HINT1 gene mutations These cause autosomal recessive axonal neuropathy with neuromyotonia Associated autoimmune disorders Associated medical disorders Associated malignancies Associated drugs and toxins Synonym
HINT1 gene mutations
- These cause autosomal recessive axonal neuropathy with neuromyotonia
Associated autoimmune disorders
Associated medical disorders
Associated malignancies
Associated drugs and toxins
Synonym
References
- Maddison P. Neuromyotonia. Clinl Neurophysiol 2006; 117:2118-2127.
- Rozevska M, Rots D, Gailite L, et al. The most common European HINT1 neuropathy variant phenotype and its case studies. Front Neurol 2023; 14:1084335.
- Peeters K, Chamova T, Tournev I, Jordanova A. Axonal neuropathy with neuromyotonia: there is a HINT. Brain 2017; 140:868-877.
- Lertnawapan R, Kulkantrakorn K. Isaacs' syndrome in a patient with dermatomyositis: case report and review of the literature. Int J Rheum Dis 2017; 20:1039-1045.
- Turner MR, Madkhana A, Ebers GC, et al. Wasp sting induced autoimmune neuromyotonia. JNNP 2006; 77:704-705.
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