Hereditary sensory and autonomic neuropathy (HSAN): type VIII
Evidence-based neurology checklist on hereditary sensory and autonomic neuropathy (hsan): type viii: Genetics This is caused by PRDM12 gene mutations The transmission is autosomal recessive Clinical features Complications Investigations Synonym Acronym
Genetics
- This is caused by PRDM12 gene mutations
- The transmission is autosomal recessive
Clinical features
Complications
Investigations
Synonym
Acronym
References
- Schwartzlow C, Kazamel M. Hereditary sensory and autonomic neuropathies: adding more to the classification. Curr Neurol Neurosci Rep 2019; 19:52.
- Pho-Iam T, Kulsirichawaroj P, Likasitwattanakul S, et al. Expanding the genetic landscape of congenital insensitivity to pain. Neurol Genet 2026; 12:e200346.
Related checklists
- Hereditary sensory and autonomic neuropathy (HSAN): classification
- Hereditary sensory and autonomic neuropathy (HSAN): type I
- 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
