| Literature DB >> 6431899 |
C Bordarier, J Aicardi, F Goutieres.
Abstract
Five patients are reported with Warburg's syndrome, characterized by: (1) congenital hydrocephalus, (2) severe neonatal neurological dysfunction, (3) abnormalities of the anterior and posterior chambers of the eyes, (4) absence of known cause, and (5) severe developmental abnormalities of cortical gyration and architectonics. Fourteen similar published cases are reviewed. The syndrome can be diagnosed during life on the conjunction of the first four features listed. Evidence is adduced that this syndrome is a genetically determined condition with an autosomal recessive mode of inheritance and with a 25% recurrence risk for offspring of the parents of an affected infant.Entities:
Mesh:
Year: 1984 PMID: 6431899 DOI: 10.1002/ana.410160112
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422