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Familial dysautonomia

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Description

Familial dysautonomia (FD) affects the development and survival of sensory, sympathetic, and parasympathetic neurons. It is a debilitating disease present from birth. Neuronal degeneration progresses throughout life. Affected individuals have gastrointestinal dysfunction, vomiting crises, recurrent pneumonia, altered sensitivity to pain and temperature perception, and cardiovascular instability. About 40% of individuals have autonomic crises. Hypotonia contributes to delay in acquisition of motor milestones. Older individuals often have a broad-based and ataxic gait that deteriorates over time. Life expectancy is decreased.

GeneReviews

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

495

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Genes

External Links

  • OMIM

    223900

  • Orphanet

    1764

  • HPO
  • Medgen

    C0013364

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