Fitzsimmons Syndrome: Spastic Paraplegia, Brachydactyly, and Cognitive Impairment

Christine M. Armour, Peter Humphreys, Raoul C. M. Hennekam, Kym M. Boycott

Research output: Contribution to journalArticleAcademicpeer-review

5 Citations (Scopus)

Abstract

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
Original languageEnglish
Pages (from-to)2254-2257
JournalAmerican journal of medical genetics. Part A
Volume149A
Issue number10
DOIs
Publication statusPublished - 2009

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