Purpose: The nonneurogenic neurogenic bladder has traditionally been b
elieved to represent a disorder of older children. We report on patien
ts in whom congenital dysfunctional voiding may be the underlying caus
e of nonneurogenic neurogenic bladder in early infancy. Materials and
Methods: We evaluated 5 male and 2 female patients newborn to 30 month
s old with dysfunctional neurogenic bladder and no evidence of neurolo
gical pathology or anatomical outflow obstruction. Presentation includ
ed prenatal hydronephrosis in 3 cases, urosepsis in 2 and failure to t
hrive in 2. Radiological and urodynamic investigations revealed thick
walled, poorly compliant bladders in 5 patients and incomplete bladder
emptying bordering on urinary retention in 2. There was significant u
pper tract pathology in all cases, including azotemia in 4, reflux in
4 and hydroureteronephrosis in 6. Due to poor bladder function, manife
sted by incomplete emptying or high storage pressures, all patients we
re initially treated with cutaneous vesicostomy. Results: Bladder appe
arance and function subsequently improved in 3 patients and vesicostom
y was reversed. Three patients with persistently thickened bladders, i
ncluding 2 with renal failure, underwent bladder augmentation. The rem
aining patient had improved bladder storage function but requires inte
rmittent catheterization. Conclusions: The nonneurogenic neurogenic bl
adder represents a rare, severe form of dysfunctional voiding that may
be present even in the neonatal period.