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hereditary sensory & autonomic neuropathy type 5
Pathology:
- loss of pain sensation in combination with other sensory &/or autonomic abnormalities
Genetics:
- associated with defect in NGF-beta
Clinical manifestations:
- loss of pain perception & impaired temperature sensitivity, ulcers, & in some cases self-mutilation
- autonomic involvement is variable
General
hereditary sensory & autonomic neuropathy
Database Correlations
OMIM 608654
References
OMIM :accession 608654