k

Differential diagnoses for Konzo are lathyrism and paraparesis apparently caused by geographical location or bad genes…go figure

The clinical symptoms are strikingly similar to those of lathyrism and also similar to tropical spastic paraparesis and hereditary spastic paraparesis, only that the latter two disorders have a slow onset. Konzo is distinct from polio which is a flaccid paralysis and most often affects a person asymmetrically.[citation needed]

Konzo is one of several tropical neuropathies. A distinct myeloneuropathy also associated to cyanogen intake from cassava is tropical ataxic neuropathy (TAN), as first described in parts of Nigeria by B. O. Osuntokun in 1968. The disease is still occurring in the same areas.

Diagnosis

The WHO has recommended three criteria for the diagnosis of konzo:[citation needed]

  • a visible symmetric spastic abnormality of gait while walking or running;
  • a history of onset of less than one week followed by a non-progressive course in a formerly healthy person;
  • bilaterally exaggerated knee or ankle jerk reflexes without signs of disease of the spine.

Depending on its severity, konzo is divided into three categories: mild when individuals are able to walk without support, moderate when individuals need one or two sticks to walk, and severe when the affected person is unable to walk unsupported.

I feel a little dumber just reading this garbage but I want the notes.

Post a Comment

Your email address will not be published. Required fields are marked *