Abstract
We describe 3 children (2 siblings aged 10 and 3 years, and 1 sporadic case aged 13
years) with cerebellar vermis defect associated with oligophrenia, congenital ataxia,
and hepatic fibrocirrhosis. Differently from what is reported in COACH syndrome, coloboma
and renal involvement were absent. Since in one patient hepatic involvement was subclinical
and early therapy seemed to prevent disease progression, the presence of liver disease
should be carefully investigated in any patient with ataxia and midline cerebellar
defects.
Key words
Cerebellar Vermis Defect - Oligophrenia - Congenital Ataxia - Hepatic Fibrocirrhosis
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Prof. Antonio Pascotto
Cattedra di Neuropsichiatria Infantile, Seconda Universita' di Napoli
Via Pansini 5
80131 Napoli
Italy
eMail: antoniopascotto@unina2.it