Fitzsimmons Syndrome: Spastic Paraplegia, Brachydactyly, and Cognitive Impairment

被引:5
作者
Armour, Christine M. [1 ]
Humphreys, Peter [2 ]
Hennekam, Raoul C. M. [3 ,4 ]
Boycott, Kym M. [1 ]
机构
[1] Childrens Hosp Eastern Ontario, Dept Genet, Ottawa, ON K1H 8L1, Canada
[2] Childrens Hosp Eastern Ontario, Div Neurol, Dept Pediat, Ottawa, ON K1H 8L1, Canada
[3] UCL, Great Ormond St Hosp Children, Inst Child Hlth, London, England
[4] Univ Amsterdam, Acad Med Ctr, Dept Pediat, NL-1105 AZ Amsterdam, Netherlands
关键词
spastic paraplegia; brachydactyly; Fitzsimmons syndrome; CONE-SHAPED EPIPHYSES; DYSARTHRIA;
D O I
10.1002/ajmg.a.33003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fitzsimmons syndrome is an infrequently described entity comprising slowly progressive spastic paraplegia, brachydactyly, and cone-shaped epiphyses, dysarthria, and low-normal intelligence. Five patients with this syndrome have been reported. The cause remains unknown. Here we describe a 16-year-old boy with Fitzsimmons syndrome. He was noted to toe-walk at age 18 months and spasticity progressed slowly into a spastic gait with contractures. He has mild dysarthria. and hypernasal speech. Brachydactyly is notable but cannot be classified into one of the recognized types. A cone-shaped epiphysis was apparent on the only available childhood radiograph. He has moderate cognitive handicap and pervasive developmental delay. A detailed comparison of this patient with the earlier described cases is presented to further delineate the condition and increase awareness of this syndrome. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:2254 / 2257
页数:4
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