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Myoclonus epilepsy of the Unverricht–Lundbor type (PME-ULD) PME-ULD is an autosomal recessive disorder that typically develops between the ages of 6 and 15 years with stimulus-sensitive myoclonus and tonic colonic seizures followed by progressive cerebellar syndrome (Lehesjoki and Koskiniemi 1998
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Biol Trace Elem Res 158, 105–112.CrossRefGoogle ScholarPubMed López-Uriarte, P, Nogués, R, Saez, G, et al
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