Familial congenital heart block and hydrops fetalis.
- 1 June 1980
- journal article
- case report
- Published by BMJ in Archives of Disease in Childhood
- Vol. 55 (6) , 479-480
- https://doi.org/10.1136/adc.55.6.479
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.Keywords
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