hereditary sensory and autonomic neuropathy type 1

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Disease Overview

Hereditary sensory neuropathy type I (HSN I) is a slowly progressive neurological disorder characterized by prominent predominantly distal sensory loss, autonomic disturbances, autosomal dominant inheritance, and juvenile or adulthood disease onset.

Synonyms

HSAN 1
HSAN1
HSN1
Hereditary Sensory Neuropathy Type I
hereditary sensory and autonomic neuropathy type I
hereditary sensory neuropathy type 1
neuropathy hereditary sensory and autonomic type 1
neuropathy hereditary sensory radicular, autosomal dominant

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.