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What is Hopkins Disease?

Published in Neurological Disorders 1 min read

Hopkins syndrome, also known as post-asthmatic amyotrophy, is a rare, poliomyelitis-like condition that primarily affects children after experiencing status asthmaticus, a severe asthma attack. Though more common in childhood, it can also occur after puberty.

Here's a breakdown of Hopkins syndrome:

  • Definition: A neurological condition characterized by rapidly progressive and permanent muscle weakness, usually affecting a single limb (monoplegia) or both limbs on one side of the body (diplegia).
  • Cause: It occurs following a severe asthma attack (status asthmaticus). The exact mechanism linking asthma and the neurological condition is not fully understood.
  • Age of Onset: Most commonly seen in children, but can occur in adults as well.
  • Key Features:
    • Sudden onset of limb weakness.
    • Paralysis that can be permanent.
    • Often affects one limb (monoplegia) or both limbs on the same side of the body (diplegia).
    • Typically follows a severe asthma attack.

In essence, Hopkins disease/syndrome describes a specific neurological complication occurring after severe asthma, resulting in limb paralysis.

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