Deafness, sensory neuropathy, and ovarian dysgenesis: A new syndrome or a broader spectrum of Perrault syndrome?

W. H.J.P. Linssen*, M. J. Van den Bent, H. G. Brunner, P. J.E. Poels

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

33 Citations (Scopus)

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 languageEnglish
Pages (from-to)81-82
Number of pages2
JournalAmerican Journal of Medical Genetics
Volume51
Issue number1
DOIs
Publication statusPublished - 15 May 1994
Externally publishedYes

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