| Literature DB >> 15216544 |
Agata Fiumara1, Giovanni Sorge, Antonio Toscano, Enrico Parano, Lorenzo Pavone, John M Opitz.
Abstract
Perrault syndrome (PS) comprises gonadal dysgenesis and sensorineural deafness in females, and deafness in affected males. More recent studies have asked whether the neurological signs in some of the patients are a coincidental finding or part of the syndrome. We report on two pairs of sisters with gonadal dysgenesis and deafness, cerebral, and ocular involvement who developed a progressive, severe sensory, and motor neuropathy. This observation constitutes further evidence of peripheral nervous system involvement in PS. Based on the clinical observations of known patients, two forms of PS may be distinguished: one apparently non-progressive form and another (exemplified by our two sets of sisters) with apparently progressive axonal-cerebellar degeneration. Copyright 2004 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2004 PMID: 15216544 DOI: 10.1002/ajmg.a.20616
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802