Hereditary sensory and autonomic neuropathy (HSAN): type I
Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .
Hereditary sensory and autonomic neuropathy (HSAN): type I. Autosomal dominant. Fully referenced neurology checklist.
Transmission
- Autosomal dominant
Subtypes
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Onset features
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Sensory features
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Orthopaedic problems
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Other features
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Occasional features
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References
- Auer-Grumbach M. Hereditary sensory neuropathy type I. Orphanet J Rare Dis 2008; 3:7.
- Houlden H, King R, Blake J, et al. Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type I (HSAN I). Brain 2006; 129:411-425.
- Klein CJ, Wu Y, Kruckeberg KE, et al. SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies. JNNP 2005; 76:1022-102.
- Schwartzlow C, Kazamel M. Hereditary sensory and autonomic neuropathies: adding more to the classification. Curr Neurol Neurosci Rep 2019; 19:52.
- Rotthier A, Baets J, De Vriendt E, et al. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain 2009; 132:2699-2711.
Related checklists
- Hereditary sensory and autonomic neuropathy (HSAN): classification
- Hereditary sensory and autonomic neuropathy (HSAN): type II
- Hereditary sensory and autonomic neuropathy (HSAN): type III
- Hereditary sensory and autonomic neuropathy (HSAN): type IV
- Hereditary sensory and autonomic neuropathy (HSAN): type V
- Hereditary sensory and autonomic neuropathy (HSAN): type VI
- Hereditary sensory and autonomic neuropathy (HSAN): type VII
- Hereditary sensory and autonomic neuropathy (HSAN): type VIII
