Perrault syndrome: Evidence for progressive nervous system involvement

被引:40
作者
Fiumara, A
Sorge, G
Toscano, A
Parano, E
Pavone, L
Opitz, JM
机构
[1] Univ Catania, Dipartimento Pediat, I-95125 Catania, Italy
[2] Univ Messina, Dept Neurol, I-98100 Messina, Italy
[3] CNR, Ist Bioimmagini & Fisiopatol Sistema Nervoso Cent, Catania, Italy
[4] Univ Utah, Dept Pediat, Salt Lake City, UT USA
[5] Univ Utah, Dept Human Genet, Salt Lake City, UT USA
[6] Univ Utah, Dept Obstet & Gynecol, Salt Lake City, UT USA
关键词
Perrault syndrome; sensorineural deafness; ovarian dysgenesis; hereditary motor sensory neuropathy;
D O I
10.1002/ajmg.a.20616
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:246 / 249
页数:4
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