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Clinical characteristics and gene variants of patients with infantile intrahepatic cholestasis / 中国当代儿科杂志
Article 在 Zh | WPRIM | ID: wpr-879815
Responsible library: WPRO
ABSTRACT
OBJECTIVE@#To explore the clinical characteristics and genetic findings of patients with infantile intrahepatic cholestasis.@*METHODS@#The clinical data were collected in children who were admitted to the Department of Gastroenterology in Children's Hospital, Capital Institute of Pediatrics from June 2017 to June 2019 and were suspected of inherited metabolic diseases. Next generation sequencing based on target gene panel was used for gene analysis in these children. Sanger sequencing technology was used to verify the genes of the members in this family.@*RESULTS@#Forty patients were enrolled. Pathogenic gene variants were identified in 13 patients (32%), including @*CONCLUSIONS@#The etiology of infantile intrahepatic cholestasis is complex. Next generation sequencing is helpful in the diagnosis of infantile intrahepatic cholestasis.
Subject(s)
全文: 1 索引: WPRIM 主要主题: Genetic Testing / Cholestasis, Intrahepatic / Alagille Syndrome / Citrullinemia / Mitochondrial Membrane Transport Proteins / High-Throughput Nucleotide Sequencing / Mutation 研究类型: Prognostic_studies 限制: Child / Humans 语言: Zh 期刊: Chinese Journal of Contemporary Pediatrics 年: 2021 类型: Article
全文: 1 索引: WPRIM 主要主题: Genetic Testing / Cholestasis, Intrahepatic / Alagille Syndrome / Citrullinemia / Mitochondrial Membrane Transport Proteins / High-Throughput Nucleotide Sequencing / Mutation 研究类型: Prognostic_studies 限制: Child / Humans 语言: Zh 期刊: Chinese Journal of Contemporary Pediatrics 年: 2021 类型: Article