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Brachytelephalangic chondrodysplasia punctata in an extremely premature infant
Authors:Wim H. J. P. Linssen  Martin J. Van den Bent  Han G. Brunner  Petra J. E. Poels
Affiliation:Department of Child Health Queen's Medical Centre
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. © 1994 Wiley-Liss, Inc.
Keywords:Perrault syndrome  sensory neuropathy  amelogenesis imperfecta
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