| Literature DB >> 1548491 |
V Leuzzi1, E Bertini, A M De Negri, M Gallucci, B Garavaglia.
Abstract
Two siblings developed a neurological disorder in the first decade characterised by generalised dystonia, hypokinesia, and subacute visual loss. CT and serial MRI examinations showed bilateral lesions of the striatum, mainly in the putamen. The classification of these patients is discussed in relation to infantile bilateral striatal necrosis (IBSN), Leigh's disease, and Leber's optic neuropathy. The literature shows a clinical and aetiopathogenetic overlap between these syndromes. In our cases parental consanguinity and the involvement of a single generation suggest a new clinical condition with autosomal recessive transmission.Entities:
Mesh:
Year: 1992 PMID: 1548491 PMCID: PMC488925 DOI: 10.1136/jnnp.55.1.16
Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN: 0022-3050 Impact factor: 10.154