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Sialidosis type I (cherry red spot-myoclonus syndrome)
Sutapa Ganguly1, Rajesh U Gabani, Sandeep Chakraborty
1Department of Paediattrics, IPGMER & SSKM Hospital, Kolkata.
Journal of the Indian Medical Association
|October 12, 2004
Abstract:
Sialidosis type 1 or the cherry red spot-myoclonus syndrome (CRSM) is an autosomal recessive disorder with the onset in adolescence of myoclonus and gradual visual failure. Here, a case of CRSM in a 12-year-old Bengali Muslim girl with the history of myoclonic jerks of limbs and the body since last 2 years and gradual impairment of vision since last one year is presented with a brief review of the literature.
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