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[Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism].

作者信息

Denys P, Malvaux P, Van Den Berghe H, Tanghe W, Proesmans W

出版信息

Arch Fr Pediatr. 1967 Aug-Sep;24(7):729-39.

PMID:4292870
Abstract
摘要

相似文献

1
[Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism].
Arch Fr Pediatr. 1967 Aug-Sep;24(7):729-39.
2
Wilms' tumor, nephron disorder and ambiguous genitalia.肾母细胞瘤、肾单位疾病与生殖器模糊。
Z Kinderchir. 1983 Oct;38(5):345-9. doi: 10.1055/s-2008-1060003.
3
The nephropathy associated with male pseudohermaphroditism and Wilms' tumor (Drash syndrome): a distinctive glomerular lesion--report of 10 cases.与男性假两性畸形和肾母细胞瘤相关的肾病(德拉斯综合征):一种独特的肾小球病变——10例报告
Clin Nephrol. 1985 Dec;24(6):269-78.
4
[Association of Wilms' tumor, pseudohermaphroditism and glomerular nephropathy. Partial and complete forms of the syndrome].[肾母细胞瘤、假性两性畸形与肾小球肾病的关联。该综合征的部分及完全形式]
Bol Med Hosp Infant Mex. 1979 Nov-Dec;36(6):1203-12.
5
Pseudohermaphroditism, glomerulonephritis with the nephrotic syndrome, and Wilms' tumor in infancy.假性两性畸形、伴有肾病综合征的肾小球肾炎以及婴儿期的肾母细胞瘤。
J Pediatr. 1971 Oct;79(4):677-81. doi: 10.1016/s0022-3476(71)80322-0.
6
Nephroblastoma associated with mesangioproliferative glomerulonephritis.
Eur Urol. 1982;8(2):125-6. doi: 10.1159/000473495.
7
[Drash syndrome].
Pediatrie. 1992;47(11):757-60.
8
Association of Wilms' tumor with Peter's anomaly.
Ann Ophthalmol. 1984 Oct;16(10):933-4.
9
Wilms tumor and nephrotic syndrome in male pseudohermaphroditism.男性假两性畸形中的肾母细胞瘤和肾病综合征
Urology. 1984 Dec;24(6):595-600. doi: 10.1016/0090-4295(84)90110-9.
10
[Wilms tumor in childhood diagnosed during therapy of acute lymphoid leukemia].[急性淋巴细胞白血病治疗期间诊断出的儿童肾母细胞瘤]
Orv Hetil. 1985 Jan 13;126(2):91-2.

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A review of the genetic background in complicated WT1-related disorders.
复杂的WT1相关疾病的遗传背景综述。
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Non-Syndromic and Syndromic Defects in Children with Extracranial Germ Cell Tumors: Data of 2610 Children Registered with the German MAKEI 96/MAHO 98 Registry Compared to the General Population.颅外生殖细胞瘤患儿的非综合征性和综合征性缺陷:与普通人群相比,德国MAKEI 96/MAHO 98登记处登记的2610名儿童的数据
Cancers (Basel). 2024 Jun 6;16(11):2157. doi: 10.3390/cancers16112157.
5
WT1-related disorders: more than Denys-Drash syndrome.WT1 相关疾病:不仅仅是 Denys-Drash 综合征。
Pediatr Nephrol. 2024 Sep;39(9):2601-2609. doi: 10.1007/s00467-024-06302-y. Epub 2024 Feb 7.
6
Bilateral Gonadal Dysgerminoma in a Phenotypic Female With 46,XY Disorder of Sexual Development: A Case Report.一名患有46,XY性发育障碍的表型女性双侧性腺无性细胞瘤:病例报告
Cureus. 2023 Apr 26;15(4):e38149. doi: 10.7759/cureus.38149. eCollection 2023 Apr.
7
New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome: A CARE-compliant case report.WT1 基因突变导致男孩出现不完全型 Denys-Drash 综合征:一项符合 CARE 原则的病例报告。
Medicine (Baltimore). 2021 May 14;100(19):e25864. doi: 10.1097/MD.0000000000025864.
8
Case Report: Denys-Drash Syndrome With Causative Variant Presenting as Atypical Hemolytic Uremic Syndrome.病例报告:伴有致病变异的迪尼-德拉斯综合征表现为非典型溶血尿毒症综合征。
Front Pediatr. 2020 Dec 18;8:605889. doi: 10.3389/fped.2020.605889. eCollection 2020.
9
Long-term outcome in a case series of Denys-Drash syndrome.一组Denys-Drash综合征病例的长期预后
Clin Kidney J. 2019 Mar 16;12(6):836-839. doi: 10.1093/ckj/sfz022. eCollection 2019 Dec.
10
Management of Denys-Drash syndrome: A case series based on an international survey.迪尼-德拉斯综合征的管理:基于国际调查的病例系列
Clin Nephrol Case Stud. 2018 Nov 12;6:36-44. doi: 10.5414/CNCS109515. eCollection 2018.