Subacute myelo-optic neuropathy

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Subacute myelo-optic neuropathy
Synonyms SMON
Pronounce N/A
Specialty N/A
Symptoms Visual impairment, paralysis, numbness
Complications Blindness, paraplegia
Onset Subacute
Duration Chronic
Types N/A
Causes Clioquinol toxicity
Risks Use of clioquinol
Diagnosis Clinical evaluation, neurological examination
Differential diagnosis Multiple sclerosis, neuromyelitis optica
Prevention N/A
Treatment Discontinuation of clioquinol, supportive care
Medication N/A
Prognosis Variable, can lead to permanent disability
Frequency Rare, historically significant in Japan
Deaths N/A


Subacute Myelo-Optic Neuropathy (SMON) is a rare, toxic disorder that was prevalent in Japan during the 1960s and 1970s. The disease is characterized by subacute onset of sensory and motor disturbances in the lower limbs, visual impairment, and, in some cases, bowel and bladder dysfunction.

Epidemiology[edit]

SMON was first recognized in Japan in the 1960s, where it reached epidemic proportions. The disease affected over 10,000 people in Japan before its cause was identified as the drug clioquinol. After the drug was withdrawn from the market, the incidence of SMON dropped dramatically.

Symptoms[edit]

The symptoms of SMON include sensory and motor disturbances in the lower limbs, visual impairment, and, in some cases, bowel and bladder dysfunction. The onset of symptoms is usually subacute, occurring over a period of days to weeks.

Cause[edit]

The cause of SMON was identified as the drug clioquinol, an antifungal and antiprotozoal medication. Clioquinol was widely used in Japan to treat various intestinal infections. However, it was found to be neurotoxic, leading to the development of SMON in some individuals.

Treatment[edit]

Treatment for SMON is primarily supportive, as there is no cure for the disease. Management of symptoms may include physical therapy for motor disturbances, visual aids for visual impairment, and medications to manage bowel and bladder dysfunction.

See also[edit]

References[edit]

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