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Riley-Day syndrome Health Article
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Definition
Riley-Day syndrome is an inherited disorder that affects the development and function of nerves throughout the body.
Alternative Names
Familial dysautonomia; Hereditary sensory and autonomic neuropathy - type III (HSAN III)
Causes, incidence, and risk factors
Riley-Day syndrome is passed down through families (inherited). A person must inherit a copy of the defective gene from each parent to develop the condition. This condition is seen most often in people of Eastern European Jewish ancestry (Ashkenazi Jews), where the incidence is 1 in 3,700. The disease is caused by a change (mutation) of the IKBKAP gene on chromosome 9. It is rare in the general population.
Symptoms
Symptoms are present at birth and grow worse over time.
Signs and tests
The health care provider will perform a physical exam. The patient may have:
Blood tests are available to check for the IKBKAP gene. The detection rate in the Ashkenazi Jewish population is greater than 99%.
Treatment
Treatment may include:
Expectations (prognosis)
With advances in diagnosis and treatment, survival continues to improve. Currently, a newborn with Riley-Day has a 50% chance of reaching age 30. |
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