Brun Brianna N, Mockler Shelley R H, Laubscher Katie M, Stephan Carrie M, Wallace Anne M, Collison Julia A, Zimmerman M Bridget, Dobyns William B, Mathews Katherine D
From the Departments of Pediatrics (B.N.B., C.M.S., J.A.C., K.D.M.) and Neurology (K.D.M.), University of Iowa Carver College of Medicine; Center for Disabilities and Development (S.R.H.M., K.M.L.), University of Iowa Children's Hospital; Department of Communication Sciences and Disorders (A.M.W.), Department of Biostatistics, College of Public Health (M.B.Z.), University of Iowa, Iowa City; Departments of Pediatrics (Genetics) (W.B.D.) and Neurology (W.B.D.), University of Washington, Seattle; and Center for Integrative Brain Research (W.B.D.), Seattle Children's Research Institute, Seattle, WA.
Neurology. 2017 Feb 14;88(7):623-629. doi: 10.1212/WNL.0000000000003609. Epub 2017 Jan 13.
To describe the spectrum of brain MRI findings in a cohort of individuals with dystroglycanopathies (DGs) and relate MRI results to function.
All available brain MRIs done for clinical indications on individuals enrolled in a DG natural history study (NCT00313677) were reviewed. Reports were reviewed when MRI was not available. MRIs were categorized as follows: (1) cortical, brainstem, and cerebellar malformations; (2) cortical and cerebellar malformations; or (3) normal. Language development was assigned to 1 of 3 categories by a speech pathologist. Maximal motor function and presence of epilepsy were determined by history or examination.
Twenty-five MRIs and 9 reports were reviewed. The most common MRI abnormalities were cobblestone cortex or dysgyria with an anterior-posterior gradient and cerebellar hypoplasia. Seven individuals had MRIs in group 1, 8 in group 2, and 19 in group 3. Language was impaired in 100% of those in MRI groups 1 and 2, and degree of language impairment correlated with severity of imaging. Eighty-five percent of the whole group achieved independent walking, but only 33% did in group 1. Epilepsy was present in 8% of the cohort and rose to 37% of those with an abnormal MRI.
Developmental abnormalities of the brain such as cobblestone lissencephaly, cerebellar cysts, pontine hypoplasia, and brainstem bowing are hallmarks of DG and should prompt consideration of these diagnoses. Brain imaging in individuals with DG helps to predict outcomes, especially language development, aiding clinicians in prognostic counseling.
描述一组肌聚糖病(DG)患者的脑磁共振成像(MRI)表现谱,并将MRI结果与功能相关联。
回顾了为参加DG自然史研究(NCT00313677)的个体进行的所有用于临床指征的脑MRI检查。当无法获取MRI时,查阅报告。MRI被分类如下:(1)皮质、脑干和小脑畸形;(2)皮质和小脑畸形;或(3)正常。语言发育由言语病理学家分为3类中的1类。通过病史或检查确定最大运动功能和癫痫的存在情况。
回顾了25份MRI检查和9份报告。最常见的MRI异常是鹅卵石样皮质或有前后梯度的发育异常脑回以及小脑发育不全。7名个体的MRI属于第1组,8名属于第2组,19名属于第3组。MRI第1组和第2组中的个体100%存在语言障碍,且语言障碍程度与影像学严重程度相关。整个组中85%的人实现了独立行走,但第1组中只有33%的人做到了。该队列中8%的人患有癫痫,在MRI异常的人中这一比例升至37%。
脑发育异常,如鹅卵石样无脑回、小脑囊肿、脑桥发育不全和脑干弯曲,是DG的特征,应促使考虑这些诊断。DG患者的脑成像有助于预测预后,尤其是语言发育,有助于临床医生进行预后咨询。