Progressive encephalopathy, developmental delay, microcephaly, electro
encephalogram (EEG) and computed tomographic (CT) scan abnormalities h
ave been reported in 80% of children with chronic renal failure (CRF)
in infancy. Malnutrition, aluminium intoxication and psychosocial depr
ivation are proposed as causes. In 15 children with CRF from infancy w
e evaluated the effect of no aluminium salts and early vigorous nutrit
ional and psychosocial support, in addition to the standard therapy, o
n neurological development. Six patients underwent dialysis (2 at birt
h) and 3 received transplants. None of our patients were given alumini
um therapy. The nutritional status of the patients in the first 2 year
s of life was assessed with the waterlow classification. At the end of
the follow-up period (mean 50 months range 14-148 months), patients u
nderwent neurodevelopmental assessment, head CT scan, EEG, nerve condu
ction velocity (NCV) and auditory brain stem evoked response (ABER). N
one of our patients developed progressive encephalopathy or recurrent
seizures. All have a normal neurological examination apart from hypoto
nia. Microcephaly was present in 5 patients. There was a good correlat
ion between malnutrition in the first 2 years of life and microcephaly
. Developmental delay was present in 3 patients; all 3 were microcepha
lic. There was evidence of brain atrophy on CT scan in only 3 patients
. EEG was abnormal in 6 patients, but only severe in 1 patient. Only 1
patient had diminished NCV; all patients had a normal ABER. We conclu
de that a policy of no oral aluminium therapy and early nutritional su
pport leads to better neurological outcome in children with CRF from i
nfancy.