| Literature DB >> 7305422 |
Abstract
A 2 1/2-year-old girl with hypomelanosis of Itô is described. There is a bizarre distribution of congenital depigmentation stopping abruptly at the midline anteriorly, with whorl-like and zig-zag patterning. As can happen in this syndrome, there is severe retardation and intractible epilepsy, with computerized tomography showing gross cerebral atrophy.Entities:
Mesh:
Year: 1981 PMID: 7305422 PMCID: PMC1627329 DOI: 10.1136/adc.56.10.798
Source DB: PubMed Journal: Arch Dis Child ISSN: 0003-9888 Impact factor: 3.791