TY - JOUR
T1 - Fitzsimmons Syndrome: Spastic Paraplegia, Brachydactyly, and Cognitive Impairment
AU - Armour, Christine M.
AU - Humphreys, Peter
AU - Hennekam, Raoul C. M.
AU - Boycott, Kym M.
PY - 2009
Y1 - 2009
N2 - 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
AB - 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
U2 - https://doi.org/10.1002/ajmg.a.33003
DO - https://doi.org/10.1002/ajmg.a.33003
M3 - Article
C2 - 19760657
SN - 1552-4825
VL - 149A
SP - 2254
EP - 2257
JO - American journal of medical genetics. Part A
JF - American journal of medical genetics. Part A
IS - 10
ER -