Novel Clinical Features in Pontine Tegmental Cap Dysplasia

被引:14
|
作者
Rudaks, Laura I. [1 ]
Patel, Sandeep [2 ]
Barnett, Christopher P. [1 ,3 ]
机构
[1] Womens & Childrens Hosp, S Australian Clin Genet Serv, Adelaide, SA 5006, Australia
[2] Med Imaging Womens & Childrens Hosp, Adelaide, SA, Australia
[3] SA Pathol Womens & Childrens Hosp, Adelaide, SA, Australia
关键词
MALFORMATION; HINDBRAIN; SPECTRUM;
D O I
10.1016/j.pediatrneurol.2012.02.032
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Pontine tegmental cap dysplasia is a rare neurologic condition first described by Barth et al. in 2007. It is characterized by a vaulted pontine tegmentum projecting into the fourth ventricle and ventral pontine hypoplasia. Patients present with developmental delay, cerebellar and pyramidal abnormalities, cranial nerve dysfunction, and various extracranial malformations. The condition is thought to occur as a result of aberrant neuronal axonal guidance during embryologic development. Its genetic etiology has not been identified. We describe a further case of this rare condition with several features not previously reported, including aortic arch hypoplasia and mirror movements. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:393 / 396
页数:4
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