| Literature DB >> 3982656 |
Abstract
We report the clinical and neuroradiologic findings and the association of a chromosome abnormality, t(2,8), with a case of hypomelanosis of Ito (incontinentia pigmenti achromians). Chromosome anomalies have not been previously recognized in this genetically determined, neurocutaneous disorder.Entities:
Mesh:
Year: 1985 PMID: 3982656 DOI: 10.1212/wnl.35.4.607
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910