Coexistence of Unverricht-Lundborg disease and congenital deafness: molecular resolution of a complex comorbidity.


PURPOSE We report on genetic analysis of a complex condition in a Serbian family of four siblings, wherein two had progressive myoclonic epilepsy (PME) and congenital deafness (CD), one had isolated congenital deafness (ICD), and one was healthy. METHODS AND RESULTS Molecular diagnosis performed by Southern blotting confirmed Unverricht-Lundborg disease… (More)
DOI: 10.1111/j.1528-1167.2008.01937.x


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