Macrocerebellum in Achondroplasia: A Further CNS Manifestation of FGFR3 Mutations?

被引:4
|
作者
Pascoe, H. M. [1 ]
Yang, J. Y-M [2 ,3 ,4 ,5 ]
Chen, J. [4 ]
Fink, A. M. [1 ,6 ]
Kumbla, S. [1 ,7 ]
机构
[1] Royal Childrens Hosp, Dept Med Imaging, 50 Flemington Rd, Parkville, Vic 3052, Australia
[2] Royal Childrens Hosp, Dept Neurosurg, Parkville, Vic, Australia
[3] Murdoch Childrens Res Inst, Dept Neurosci Res, Parkville, Vic, Australia
[4] Murdoch Childrens Res Inst, Dept Dev Imaging, Parkville, Vic, Australia
[5] Univ Melbourne, Dept Paediat, Parkville, Vic, Australia
[6] Mercy Hosp Women, Dept Perinatal Med, Heidelberg, Vic, Australia
[7] Monash Hlth, Dept Diagnost Imaging, Clayton, Vic, Australia
关键词
NEUROIMAGING FINDINGS; BRAIN; CHILDREN;
D O I
10.3174/ajnr.A6369
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Achondroplasia is the result of a mutation in the fibroblast growth factor receptor 3 gene (FGFR3). Appearances suggestive of macrocerebellum have not been described in this patient group. We retrospectively reviewed MR imaging studies of the brain in 23 children with achondroplasia. A constellation of imaging findings that are recognized in macrocerebellum was observed, including cerebellar hemisphere enlargement (inferior and superior extension, wrapping around the brainstem); an effaced retro- and infravermian cerebellar subarachnoid CSF space; a shortened midbrain; distortion of the tectal plate; and mass effect on the brainstem. All MR imaging studies exhibited some of these findings. Quantitative analysis confirmed an increased cerebellar volume compared with age- and sex-matched controls. We hypothesized that this may be due to direct effects of the FGFR3 mutation on cerebellar morphogenesis.
引用
收藏
页码:338 / 342
页数:5
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