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.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 287-291 |
| Numero di pagine | 5 |
| Rivista | American Journal of Medical Genetics |
| Volume | 28 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 1987 |
Keywords
- syndrome
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