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 |
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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 |