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一名患有与膈肌缺损相关的丹尼斯-德拉什综合征患者出现胸腔积液。

Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect.

作者信息

Cho Hee Yeon, Lee Byong Sop, Kang Chang Hyun, Kim Woong-Han, Ha Il Soo, Cheong Hae Il, Choi Young

机构信息

Department of Pediatrics, Seoul National University Children's Hospital, 28 Yongon-dong, Chongro-gu, Seoul 110-744, South Korea.

出版信息

Pediatr Nephrol. 2006 Dec;21(12):1909-12. doi: 10.1007/s00467-006-0273-5. Epub 2006 Aug 25.

DOI:10.1007/s00467-006-0273-5
PMID:16932893
Abstract

The Wilms tumor suppressor gene, WT1, plays an important role in the development of the urogenital system and the gonads, and clinical syndromes associated with WT1 mutations, such as WAGR syndrome, Denys-Drash syndrome and Frasier syndrome, typically manifest as renal and genitourinary abnormalities. WT1 may also play an important role in the development of the diaphragm, and recently several papers have reported an association between WT1 mutations and diaphragmatic hernias. In addition, WT1 mutations were also detected in some patients with Meacham syndrome, a rare malformation syndrome comprising congenital diaphragmatic hernia, double vagina, sex reversal, and cardiac malformations. Here, we report a case of an infant with typical clinical features of Deny-Drash syndrome and a heterozygous missense mutation, Arg366His, in the WT1 gene, in whom a diaphragm defect was detected after starting peritoneal dialysis. Diaphragmatic defects are rare but may be considered as clinical manifestations of WT1 mutation syndromes. In addition, we suggest that WT1 abnormalities should be suspected in patients with chronic renal failure who develop hydrothorax after peritoneal dialysis, especially in those with genitourinary abnormalities.

摘要

威尔姆斯肿瘤抑制基因WT1在泌尿生殖系统和性腺发育中起重要作用,与WT1突变相关的临床综合征,如WAGR综合征、迪尼-德拉斯综合征和弗雷泽综合征,通常表现为肾脏和泌尿生殖系统异常。WT1在膈肌发育中可能也起重要作用,最近有几篇论文报道了WT1突变与膈肌疝之间的关联。此外,在一些患有米查姆综合征的患者中也检测到WT1突变,米查姆综合征是一种罕见的畸形综合征,包括先天性膈肌疝、双阴道、性反转和心脏畸形。在此,我们报告一例患有迪尼-德拉斯综合征典型临床特征且WT1基因存在杂合错义突变(Arg366His)的婴儿病例,该婴儿在开始腹膜透析后被检测出膈肌缺陷。膈肌缺陷很少见,但可被视为WT1突变综合征的临床表现。此外,我们建议,对于在腹膜透析后出现胸腔积液的慢性肾衰竭患者,尤其是伴有泌尿生殖系统异常的患者,应怀疑存在WT1异常。

相似文献

1
Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect.一名患有与膈肌缺损相关的丹尼斯-德拉什综合征患者出现胸腔积液。
Pediatr Nephrol. 2006 Dec;21(12):1909-12. doi: 10.1007/s00467-006-0273-5. Epub 2006 Aug 25.
2
A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome.一名被诊断为迪尼斯-德拉斯综合征的新生儿中发现的一种新型WT1基因突变。
Genet Couns. 2012;23(2):255-61.
3
Denys-Drash syndrome and congenital diaphragmatic hernia: another case with the 1097G > A(Arg366His) mutation.迪尼-德拉斯综合征与先天性膈疝:另一例携带1097G > A(精氨酸366组氨酸)突变的病例。
Am J Med Genet A. 2008 Feb 15;146A(4):496-9. doi: 10.1002/ajmg.a.32168.
4
WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations.米查姆综合征中的WT1突变提示心脏和膈肌畸形起源于体腔间皮。
Am J Med Genet A. 2007 Oct 1;143A(19):2312-20. doi: 10.1002/ajmg.a.31924.
5
Congenital diaphragmatic hernia in WAGR syndrome.WAGR综合征中的先天性膈疝。
Am J Med Genet A. 2005 May 1;134(4):430-3. doi: 10.1002/ajmg.a.30654.
6
Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome.基于长期保存组织对先天性肾病综合征诊断的优化:c.1097G>A(p.(Arg366His))WT1突变导致迪尼-德拉斯综合征
Fetal Pediatr Pathol. 2016;35(2):112-9. doi: 10.3109/15513815.2016.1139018. Epub 2016 Feb 16.
7
Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene.由于WT1基因中c.1097G>A突变导致的单卵双胞胎患Denys-Drash综合征并伴有新生儿肾衰竭。
Fetal Pediatr Pathol. 2011;30(4):266-72. doi: 10.3109/15513815.2011.555814. Epub 2011 Mar 24.
8
An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.WT1基因IVS9 +4C>T突变导致的弗雷泽综合征异常表型:主要为男性生殖器模糊且无性腺发育不全
J Clin Endocrinol Metab. 2002 Jun;87(6):2500-5. doi: 10.1210/jcem.87.6.8521.
9
Case report: WT1 exon 6 truncation mutation and ambiguous genitalia in a patient with Denys-Drash syndrome.病例报告:一名患有迪尼斯-德拉斯综合征的患者出现WT1基因外显子6截断突变及生殖器模糊不清的情况。
Curr Opin Pediatr. 2008 Feb;20(1):103-6. doi: 10.1097/MOP.0b013e3282f357eb.
10
Denys-Drash syndrome.迪尼-德拉斯综合征
Medicina (Kaunas). 2005;41(2):132-4.

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Pediatr Nephrol. 2025 Mar 3. doi: 10.1007/s00467-025-06713-5.
2
Role of genetics and the environment in the etiology of congenital diaphragmatic hernia.遗传与环境在先天性膈疝病因学中的作用。
World J Pediatr Surg. 2024 Aug 21;7(3):e000884. doi: 10.1136/wjps-2024-000884. eCollection 2024.
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The Role of Variants in Patients with Congenital Diaphragmatic Hernia.变异在先天性膈疝患者中的作用。

本文引用的文献

1
Immunohistochemical diagnosis of epithelioid mesothelioma: an update.上皮样间皮瘤的免疫组织化学诊断:最新进展
Arch Pathol Lab Med. 2005 Nov;129(11):1407-14. doi: 10.5858/2005-129-1407-IDOEMA.
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WAGR syndrome: a clinical review of 54 cases.WAGR综合征:54例临床回顾
Pediatrics. 2005 Oct;116(4):984-8. doi: 10.1542/peds.2004-0467.
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Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program.基于医院的畸形监测项目中,患有博赫dalek氏膈肌疝的婴儿:同胞复发和单卵双胞胎不一致情况
Genes (Basel). 2021 Sep 11;12(9):1405. doi: 10.3390/genes12091405.
4
Management of Congenital Diaphragmatic Hernia (CDH): Role of Molecular Genetics.先天性膈疝(CDH)的管理:分子遗传学的作用。
Int J Mol Sci. 2021 Jun 14;22(12):6353. doi: 10.3390/ijms22126353.
5
Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin.一位女孩在未公开摄入生物素的情况下出现 Denys-Drash 综合征的不寻常表现。
J Clin Res Pediatr Endocrinol. 2021 Aug 23;13(3):347-352. doi: 10.4274/jcrpe.galenos.2020.2020.0064. Epub 2020 Aug 25.
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The influence of genetics in congenital diaphragmatic hernia.遗传学对先天性膈疝的影响。
Semin Perinatol. 2020 Feb;44(1):151169. doi: 10.1053/j.semperi.2019.07.008. Epub 2019 Aug 1.
7
Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.WT1肾小球病儿科患者的基因型-表型分析
Pediatr Nephrol. 2017 Jan;32(1):81-89. doi: 10.1007/s00467-016-3395-4. Epub 2016 Jun 14.
8
Renal failure from birth-AKI or CKD? Answers.先天性肾衰竭——急性肾损伤还是慢性肾脏病?答案。
Pediatr Nephrol. 2016 Dec;31(12):2259-2262. doi: 10.1007/s00467-016-3332-6. Epub 2016 Feb 18.
9
Chronic peritoneal dialysis in children.儿童慢性腹膜透析
Int J Nephrol Renovasc Dis. 2015 Oct 7;8:125-37. doi: 10.2147/IJNRD.S82419. eCollection 2015.
10
Pleuro-peritoneal or pericardio-peritoneal leak in children on chronic peritoneal dialysis-A survey from the European Paediatric Dialysis Working Group.慢性腹膜透析儿童的胸膜-腹膜或心包-腹膜渗漏——欧洲儿科透析工作组的一项调查
Pediatr Nephrol. 2015 Nov;30(11):2021-7. doi: 10.1007/s00467-015-3137-z. Epub 2015 Jun 9.
Am J Med Genet A. 2005 Oct 1;138A(2):81-8. doi: 10.1002/ajmg.a.30904.
4
Congenital diaphragmatic hernia in WAGR syndrome.WAGR综合征中的先天性膈疝。
Am J Med Genet A. 2005 May 1;134(4):430-3. doi: 10.1002/ajmg.a.30654.
5
Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization.先天性膈疝与15号染色体长臂26区:运用荧光原位杂交和基于芯片的比较基因组杂交技术确定候选区域
Am J Hum Genet. 2005 May;76(5):877-82. doi: 10.1086/429842. Epub 2005 Mar 4.
6
Double vagina with sex reversal, congenital diaphragmatic hernia, pulmonary and cardiac malformations--another case of Meacham syndrome.
Clin Dysmorphol. 2002 Jan;11(1):25-8. doi: 10.1097/00019605-200201000-00005.
7
Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins.
Pediatr Nephrol. 2001 Mar;16(3):227-31. doi: 10.1007/s004670000537.
8
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis.WT1剪接位点突变很少与原发性类固醇抵抗性局灶节段性肾小球硬化相关。
Kidney Int. 2000 May;57(5):1868-72. doi: 10.1046/j.1523-1755.2000.00036.x.
9
Donor splice-site mutations in WT1 are responsible for Frasier syndrome.WT1基因的供体剪接位点突变是弗雷泽综合征的病因。
Nat Genet. 1997 Dec;17(4):467-70. doi: 10.1038/ng1297-467.
10
A clinical overview of WT1 gene mutations.WT1基因突变的临床概述。
Hum Mutat. 1997;9(3):209-25. doi: 10.1002/(SICI)1098-1004(1997)9:3<209::AID-HUMU2>3.0.CO;2-2.