神经母细胞瘤扩增序列缺陷继发急性肝衰竭 - Suppr

Acute Liver Failure Secondary to Neuroblastoma Amplified Sequence Deficiency.

作者信息

Cardenas Vanessa, DiPaola Frank, Adams Stacie D, Holtz Alexander M, Ahmad Ayesha

机构信息

Division of Gastroenterology, Department of Pediatrics and Communicable Diseases, C.S. Mott Children's Hospital, University of Michigan, Ann Arbor, MI.

出版信息

J Pediatr. 2017 Jul;186:179-182. doi: 10.1016/j.jpeds.2017.03.040. Epub 2017 Apr 12.

DOI:10.1016/j.jpeds.2017.03.040

PMID:28410752

Abstract

摘要

相似文献

Acute Liver Failure Secondary to Neuroblastoma Amplified Sequence Deficiency.神经母细胞瘤扩增序列缺陷继发急性肝衰竭

J Pediatr. 2017 Jul;186:179-182. doi: 10.1016/j.jpeds.2017.03.040. Epub 2017 Apr 12.

Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children.神经母细胞瘤扩增序列基因突变：儿童复发性肝衰竭的罕见病因。

Saudi J Gastroenterol. 2017 May-Jun;23(3):206-208. doi: 10.4103/1319-3767.207714.

Severe form of neuroblastoma amplified sequence deficiency in an infant with recurrent acute liver failure.一名患有复发性急性肝衰竭的婴儿的神经母细胞瘤严重形式的扩增序列缺陷。

Pediatr Int. 2018 Mar;60(3):302-304. doi: 10.1111/ped.13476.

Liver involvement in neuroblastoma amplified sequence gene deficiency is not limited to acute injury: Fibrosis silently continues.神经母细胞瘤扩增序列基因缺陷的肝损伤不仅限于急性损伤：纤维化仍在持续。

Liver Int. 2021 Oct;41(10):2433-2439. doi: 10.1111/liv.15038. Epub 2021 Aug 26.

Genomic profile of MYCN non-amplified neuroblastoma and potential for immunotherapeutic strategies in neuroblastoma.MYCN 非扩增型神经母细胞瘤的基因组特征及神经母细胞瘤免疫治疗策略的潜力。

BMC Med Genomics. 2020 Nov 10;13(1):171. doi: 10.1186/s12920-020-00819-5.

Acute Liver Failure Meets SOPH Syndrome: A Case Report on an Intermediate Phenotype.急性肝衰竭合并SOPH综合征：一例中间型表型病例报告

Pediatrics. 2017 Jan;139(1). doi: 10.1542/peds.2016-0550.

Infantile fever-triggered acute liver failure caused by novel neuroblastoma amplified sequence mutations: a case report.婴儿发热诱发的新型神经母细胞瘤扩增序列突变相关性急性肝衰竭：1 例报告。

BMC Gastroenterol. 2020 Sep 21;20(1):308. doi: 10.1186/s12876-020-01451-4.

[Exertional heat stroke caused severe hepatic and renal failure. Liver dialysis by means of MARS tested for the first time in this setting].

Lakartidningen. 2006;103(26-27):2050-3.

[Use of albumin dialysis with the MARS device to treat a case acute liver failure after partial hepatic resection].[应用分子吸附再循环系统（MARS）白蛋白透析治疗肝部分切除术后急性肝衰竭1例]

Med Clin (Barc). 2004 Jul 3;123(5):198-9. doi: 10.1016/s0025-7753(04)74458-9.

Etiology, outcome and prognostic indicators of childhood fulminant hepatic failure in the United kingdom.英国儿童暴发性肝衰竭的病因、结局及预后指标

J Pediatr Gastroenterol Nutr. 2005 May;40(5):575-81. doi: 10.1097/01.mpg.0000158524.30294.e2.

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Hepatic Phenotype in NBAS-Associated Disease: Clinical Course, Prognostic Factors and Outcome in 230 Patients.NBAS相关疾病的肝脏表型：230例患者的临床病程、预后因素及结局

Liver Int. 2025 Jul;45(7):e70146. doi: 10.1111/liv.70146.

Pregnancy, delivery, and postpartum period in infantile liver failure syndrome type 2 due to variants in .由于……中的变异导致的2型婴儿肝衰竭综合征的妊娠、分娩及产后时期

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Complex Multisystem Phenotype With Immunodeficiency Associated With Mutations: Reports of Three Patients and Review of the Literature.伴有免疫缺陷的复杂多系统表型与突变相关：三例患者报告及文献综述

Front Pediatr. 2020 Sep 15;8:577. doi: 10.3389/fped.2020.00577. eCollection 2020.

Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patients.在 110 名患者中定义 NBAS 相关疾病的临床亚组和基因型-表型相关性。

Genet Med. 2020 Mar;22(3):610-621. doi: 10.1038/s41436-019-0698-4. Epub 2019 Nov 25.

NBAS mutations cause acute liver failure: when acetaminophen is not a culprit.NBAS 突变可导致急性肝衰竭：此时并非乙酰氨基酚引起的。

Ital J Pediatr. 2017 Sep 25;43(1):88. doi: 10.1186/s13052-017-0406-4.

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Acute Liver Failure Secondary to Neuroblastoma Amplified Sequence Deficiency.

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