婴儿Joubert综合征的不寻常表现:一个案例研究

Susheel kumar saini, A. Singla, Vayom Thapar, Ajay kumar saini, S. Kumari
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摘要

Joubert综合征(JS)是一种罕见的常染色体隐性遗传病,表现为小脑蚓部发育不全并伴有复杂的脑干畸形。Joubert综合征的特点是发作性呼吸异常、动眼肌、张力低下、共济失调、发育迟缓。脑轴向磁共振显示特征性的磨牙征。由于其表型多变,临床上难以诊断。确切的诊断通常要在出生后几年才能做出。我们报告一个不寻常的朱伯特综合征的表现在一个5个月大的男孩谁提出了儿童门诊发育迟缓,身体的音调增加和头部大小异常。脑MRI显示小脑上蒂臼齿结构,第四脑室形状似蝙蝠翼,蚓部发育不全,导致两个小脑半球正中入路。
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An Unusual Presentation of Joubert Syndrome in an Infant: A Case Study
Joubert syndrome (JS) is a rare autosomal recessive disorder which show’s cerebellar vermis hypoplasia with a complex brainstem malformation. Joubert syndrome is characterized by episodes of abnormal respiratory pattern, oculomotor findings, hypotonia, ataxia, developmental retardation. Axial magnetic resonance images of brain show characteristic molar tooth sign. This syndrome is difficult to diagnose clinically because of its variable phenotype. The exact diagnosis is often not made for several years after birth. We report an unusual presentation of Joubert syndrome in a 5 month old boy who presented to the pediatric outpatient clinic with developmental delay, increase in tone of body and abnormal head size. MRI Brain showed molar tooth configuration of superior cerebellar peduncles, the fourth ventricle shaped like a bat wing and hypoplasia of the vermis which resulted in median approach of the two cerebellar hemispheres.
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