Familial dysautonomia
What is Familial dysautonomia?
A rare hereditary sensory and autonomic neuropathy characterized by decreased pain and temperature perception, absent deep tendon reflexes, proprioceptive ataxia, afferent baroreflex failure and progressive optic neuropathy.
Other condition names
- HSAN3
- Hereditary sensory and autonomic neuropathy type 3
- Hereditary sensory and autonomic neuropathy type III
- Riley-Day syndrome
Inheritance type
Autosomal recessive
Age of Onset
- Childhood
- Infancy
- Neonatal
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