Al-Smair Ali, Younes Sara, Saadeh Ahmad, Kaoukji Abdel Rahman, Jaber Osama
Medray International Radiology Center, Amman, Jordan.
Faculty of Medicine, The University of Jordan, Amman, Jordan.
Radiol Case Rep. 2022 Jul 30;17(10):3630-3634. doi: 10.1016/j.radcr.2022.07.038. eCollection 2022 Oct.
Joubert syndrome is a rare heterogeneous disease affecting the cerebellum. It usually presents with hypotonia, abnormal breathing pattern, with distinctive cerebellar and brain stem malformation called the molar tooth sign. It may present with different organ involvement or with other neurological alterations such as Dandy-Walker syndrome. Joubert syndrome with dandy walker syndrome is called Joubert-Plus syndrome, an exceedingly rare entity. Dandy-Walker syndrome is defined by hypoplasia and upward rotation of the cerebellar vermis and cystic dilation of the fourth ventricle. Atretic cephalocele is another rare diagnosis which is characterized by a herniation of intracranial contents through a skull defect. Herein, we present a case of a 6-month-old patient who presented with floppiness and a scalp nodule. After further evaluation, he was diagnosed with Joubert-Plus syndrome with an atretic cephalocele.
乔伯特综合征是一种影响小脑的罕见异质性疾病。它通常表现为肌张力减退、异常呼吸模式,并伴有称为磨牙征的独特小脑和脑干畸形。它可能伴有不同器官受累或出现其他神经系统改变,如丹迪-沃克综合征。合并丹迪-沃克综合征的乔伯特综合征称为乔伯特加综合征,是一种极其罕见的病症。丹迪-沃克综合征的定义是小脑蚓部发育不全并向上旋转以及第四脑室囊性扩张。闭锁性脑膨出是另一种罕见的诊断,其特征是颅内内容物通过颅骨缺损突出。在此,我们报告一例6个月大的患者,该患者表现为身体松软和头皮结节。经过进一步评估,他被诊断为合并闭锁性脑膨出的乔伯特加综合征。