A case of pontine tegmental cap dysplasia with comorbidity of oculoauriculovertebral spectrum

被引:14
|
作者
Chong, Pin Fee [1 ]
Haraguchi, Kohei [1 ]
Torio, Michiko [2 ]
Kirino, Makiko [3 ]
Ogata, Reina [1 ]
Matsukura, Masaru [1 ]
Sakai, Yasunari [2 ]
Ishizaki, Yoshito [2 ]
Yamamoto, Toshiyuki [4 ]
Kira, Ryutaro [1 ]
机构
[1] Fukuoka Childrens Hosp, Dept Pediat Neurol, Fukuoka 8100063, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Pediat, Fukuoka 812, Japan
[3] Kyushu Med Ctr, Dept Pediat, Fukuoka, Japan
[4] Tokyo Womens Med Univ, Inst Integrated Med Sci, Tokyo, Japan
来源
BRAIN & DEVELOPMENT | 2015年 / 37卷 / 01期
关键词
Pontine tegmental cap dysplasia; PTCD; Oculoauriculovertebral spectrum; OAVS; Pontine malformation; AURICULO-VERTEBRAL SPECTRUM; GOLDENHAR SYNDROME; ABNORMALITIES;
D O I
10.1016/j.braindev.2014.02.007
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 (PTCD) is a newly described brainstem malformation with distinct neuroimaging findings, characterized by a flattened ventral pons, cerebellar vermal hypoplasia and vaulted pontine tegmentum that forms a "caplike" or "beaklike" bulge projecting into the fourth ventricle. We describe a 3-month-old infant male who presented with typical neuroradiological findings as well as clinical features of PTCD. Notably, he manifested multiple anomalies with left ocular and facial hypoplasia, bilateral sensorineural hearing loss and rib and vertebral anomalies. Oculoauriculovertebral spectrum (OAVS) was thus considered to be an accompanying phenotype of this patient. The unique comorbidity seen in this patient suggests that PTCD and OAVS may partly share a common mechanism in their pathogenesis. (C) 2014 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:171 / 174
页数:4
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