Abstract
We report on 3 sibs (2 males and one female) with sensorineural deafness. The presence of ovarian dysgenesis in the girl suggested a diagnosis of Perrault syndrome. In addition our patients have a sensory polyneuropathy and amelogenesis imperfecta. Two of the patients have mild mental retardation, fine choreatic movements, and dyspraxia. It is discussed whether these findings are part of a separate clinical entity or should be included within the spectrum of the Perrault syndrome.
| Original language | English |
|---|---|
| Pages (from-to) | 81-82 |
| Number of pages | 2 |
| Journal | American Journal of Medical Genetics |
| Volume | 51 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 15 May 1994 |
| Externally published | Yes |