一例罕见的左半身轻瘫婴儿：双侧开放性唇裂脑畸形病例报告
A Rare Case of an Infant with Left Hemiparesis: A Case Report of Bilateral Open-lip Schizencephaly.
作者信息
Siti B C, Zulkifli M M, Mohd Yusoff S S, Muhamad R, Ahmad T M
机构信息
Klinik Kesihatan Pengkalan Kubor, Tumpat, Kelantan, Malaysia.
Department of Family Medicine, Universiti Sains Malaysia, Kubang Kerian, Malaysia, Email:
出版信息
Malays Fam Physician. 2020 Nov 10;15(3):90-94. eCollection 2020.
Schizencephaly is a very rare congenital birth defect. It is characterized by a cortical brain malformation that manifests as a grey-matter-lined cleft extending from the ependyma to the pia mater. It is a rare condition, and few cases have been reported in the literature. The exact cause is unknown. Herein, we report a case of an infant presenting with left side hemiparesis. The CT scan of her brain revealed right fronto-temporal and left parieto-temporal open-lip schizencephaly; thus, urgent referral to a pediatric neurologist was made for early intervention.
脑裂畸形是一种非常罕见的先天性出生缺陷。其特征是皮质脑畸形，表现为从室管膜延伸至软脑膜的灰质内衬裂隙。这是一种罕见病症，文献中报道的病例很少。确切病因尚不清楚。在此，我们报告一例表现为左侧偏瘫的婴儿病例。她的脑部CT扫描显示右侧额颞叶和左侧顶颞叶开放性唇裂脑裂畸形；因此，紧急转诊给儿科神经科医生进行早期干预。
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