Bobble-head doll syndrome is known to be associated with aqueductal st
enosis or cystic lesions of the III ventricle. The direction of moveme
nt is usually vertical. In the literature, only five cases of purely h
orizontal movement have been reported. Bobble-head doll syndrome manif
ested as a sign of shunt malfunction has been described in one case wi
th a ventriculoperitoneal shunt. The authors report on a 10-year-old b
oy who showed subduroperitoneal shunt malfunction associated with hori
zontal bobble-head doll syndrome. The head bobbing disappeared immedia
tely after shunt revision. Unlike the previously reported cases, in th
e present case the lesion was asymmetric, though the significance of t
his for the lateral movement is not clear. This case also showed more
marked ventricular dilatation on subduroperitoneal shunt malfunction t
han in the pre-shunt state, The underlying mechanism of the ventricula
r dilatation is unknown.