Case report of early-onset leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
10.3760/cma.j.cn101070-20201024-01657
- VernacularTitle:早发型伴脑干和脊髓受累及乳酸升高的脑白质病1例
- Author:
Pan ZHAO
1
;
Jinjin DING
;
Peichao TIAN
;
Yue WANG
;
Caifang FAN
;
Zijing MAI
Author Information
1. 郑州大学第一附属医院儿科，郑州 450052
- Keywords:
Leukoencephalopathy;
Brainstem and spinal cord involvement;
Lactate elevation;
Early-onset;
DARS2 gene
- From:
Chinese Journal of Applied Clinical Pediatrics
2022;37(7):546-549
- CountryChina
- Language:Chinese
-
Abstract:
Clinical data of a child with leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) diagnosed in the First Affiliated Hospital of Zhengzhou University in June 2020 were retrospectively analyzed.A female patient with 1 year and 2 months old presented with 10 months of developmental delay and 1 month of recurrent seizures.Physical examinations showed grade Ⅲ muscle strength of limbs, slightly higher muscle tone, active reflex of bilateral knee tendons, normal reflex of bilateral achilles tendons, and positive Babinski sign.Brain magnetic resonance imaging (MRI) showed bilateral cerebral hemisphere atrophy and diffuse abnormal signals.The whole exome sequencing test showed two heterozygous mutations of the DARS2 gene in the present case.There are no reports of early-onset LBSL gene mutation in Chinese population.A total of 6 related foreign literatures have been reported.All affected cases present psychomotor development disorders and other encephalopathy manifestations.Brain MRI involvement and DARS2 gene mutations are found in previous reports.Therefore, for children with developmental retardation, epilepsy, and diffuse abnormal signals in both cerebral hemispheres examined by brain MRI, genetic testing is recommended to confirm the diagnosis, guide prenatal diagnosis and genetic counseling.
