Neri G, Genuardi M, Natoli G, Costa P, Maggioni G
Istituto di Genetica Umana, Facoltà di Medicina A. Gemelli, U.C.S.C., Rome, Italy.
Am J Med Genet. 1987 Oct;28(2):287-91. doi: 10.1002/ajmg.1320280204.
We report on a female patient with G syndrome. The clinical expression is relatively severe and includes 2 manifestations not previously reported, ie, agenesis of the corpus callosum and umbilical hernia. These new findings support the notion that there is a developmental defect of the midline as the basis of the G syndrome.