Sleepwalking - Nomenclature, Classification, and Codification

Nomenclature, Classification, and Codification

According to a study by Dr. Christina A. Gurnett, of the Washington University School of Medicine's Department of Neurology, sleepwalking may be inherited as an autosomal dominant disorder with reduced penetrance. Genome-wide multipoint parametric linkage analysis for sleepwalking revealed a maximum logarithm of the odds score of 3.44 at chromosome 20q12-q13.12 between 55.6 and 61.4 cM.

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