Abstract
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.
Original language | English |
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Pages (from-to) | 287-291 |
Number of pages | 5 |
Journal | American Journal of Medical Genetics |
Volume | 28 |
DOIs | |
Publication status | Published - 1987 |
Keywords
- syndrome