Purpose: Giggle incontinence, the second most common type of childhood
enuresis unrelated to disease, is notoriously difficult to treat. How
ever, the association of laughter or emotion precipitated alteration o
f muscle tone is suggestive of a functional relationship to cataplexy,
a part of the narcoleptic syndrome complex that may respond to stimul
ant medication. Materials and Methods: Two boys and 5 girls (mean age
10.9 years) with giggle incontinence, a positive family history of gig
gle incontinence (4 patients) and no evidence of urological disease we
re treated with methylphenidate for 1 to 5 years. Results: All patient
s responded positively with complete cessation of enuresis to varying
dose schedules of methylphenidate. Conclusions: These results suggest
that giggle incontinence is a centrally mediated and likely hereditary
disorder that may share a common pathophysiological basis with the na
rcolepsy/ cataplexy syndrome.