Novel compound heterozygous variants in the PCCB gene causing adult-onset propionic acidemia presenting with neuropsychiatric symptoms: a case report and literature review

被引:0
|
作者
Yingxuan Li
Miaomiao Wang
Zhaoyang Huang
Jing Ye
Yuping Wang
机构
[1] Capital Medical University,Department of Neurology, Xuanwu Hospital
[2] The Beijing Key Laboratory of Neuromodulation,undefined
来源
BMC Medical Genomics | / 15卷
关键词
Adult-onset propionic acidemia; Neuropsychiatric symptoms; gene; Compound heterozygous mutation; Case report;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [21] LMNB1-Related Adult-Onset Autosomal Dominant Leukodystrophy Presenting as Movement Disorder: A Case Report and Review of the Literature
    Zhang, Yanyan
    Li, Jie
    Bai, Rong
    Wang, Jianping
    Peng, Tao
    Chen, Lijie
    Wang, Jingtao
    Liu, Yanru
    Tian, Tian
    Lu, Hong
    FRONTIERS IN NEUROSCIENCE, 2019, 13
  • [22] Novel GLDC Compound Heterozygous Variant Leading to Nonketotic Hyperglycinemia: Case Report and Literature Review
    Cao, Yanyan
    Meng, Lingzhi
    Zhang, Yudong
    Jiao, Jiancheng
    Pu, Weicong
    Ma, Li
    FRONTIERS IN PEDIATRICS, 2021, 9
  • [23] Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review
    Zhang, Zhaorui
    Yang, Zhen
    Chen, Mei
    Li, Yuzhu
    MEDICINE, 2022, 101 (42) : E31221
  • [24] A Chinese newborn with Zellweger syndrome and compound heterozygous mutations novel in the PEX1 gene: a case report and literature review
    Lu, Pei
    Ma, Li
    Sun, Jingjing
    Gong, Xiaohui
    Cai, Cheng
    TRANSLATIONAL PEDIATRICS, 2021, 10 (02) : 446 - 453
  • [25] Identification of a Compound Heterozygous LMF1 Variants in a Patient with Severe Hypertriglyceridemia - Case Report and Literature Review
    Cao, Conghui
    Liu, Yuqi
    Liu, Lu
    Wang, Xiaoli
    JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS, 2024, 31 (07) : 1106 - 1111
  • [26] Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review
    Zhou, Zhaowei
    Ma, Lidan
    Zhou, Juan
    Song, Zhijian
    Zhang, Jinmai
    Wang, Ke
    Chen, Boyu
    Pan, Dun
    Li, Zhiqiang
    Li, Changgui
    Shi, Yongyong
    BMC MEDICAL GENETICS, 2018, 19
  • [27] Novel compound heterozygous mutations of the NPC1 gene associated with Niemann-pick disease type C: a case report and review of the literature
    Chaoxin Tao
    Min Zhao
    Xiaohui Zhang
    Jihong Hao
    Qiuyue Huo
    Jie Sun
    Jiangtao Xing
    Yuna Zhang
    Jianhong Zhao
    Huaipeng Huang
    BMC Infectious Diseases, 24
  • [28] Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review
    Kettwig, Matthias
    Elpeleg, Orly
    Wegener, Eike
    Dreha-Kulaczewski, Steffi
    Henneke, Marco
    Gaertner, Jutta
    Huppke, Peter
    BMC NEUROLOGY, 2016, 16
  • [29] Novel Frameshift Heterozygous Mutation in UBAP1 Gene Causing Spastic Paraplegia-80: Case Report With Literature Review
    Zhang, Chao
    Zhu, Xiaowei
    Zhu, Zeyu
    Ni, Ruilong
    Liu, Taotao
    Zheng, Haoran
    Liu, Shihua
    Cao, Li
    Zhong, Ping
    Tian, Wotu
    FRONTIERS IN NEUROLOGY, 2022, 13
  • [30] Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review
    Matthias Kettwig
    Orly Elpeleg
    Eike Wegener
    Steffi Dreha-Kulaczewski
    Marco Henneke
    Jutta Gärtner
    Peter Huppke
    BMC Neurology, 16