CONGENITAL ANOMALY PRESENTING AS LUMP ABDOMEN IN ADOLESCENT GIRL.
作者信息
Harjai M M, Singh K J, Gill M, Nagpal B M, Singh Y
机构信息
Reader in Surgery & Paediatric Surgeon, Pune - 411 040.
Graded Specialist in Surgery, 153 GH, C/o 56 APO.
出版信息
Med J Armed Forces India. 2001 Jan;57(1):56-8. doi: 10.1016/S0377-1237(01)80094-0. Epub 2011 Jul 21.
Abstract
摘要
相似文献
1
CONGENITAL ANOMALY PRESENTING AS LUMP ABDOMEN IN ADOLESCENT GIRL.青春期女孩以腹部肿块为表现的先天性异常
Med J Armed Forces India. 2001 Jan;57(1):56-8. doi: 10.1016/S0377-1237(01)80094-0. Epub 2011 Jul 21.
2
Mayer-Rokitansky-Küster-Hauser syndrome accompanied by renal cell carcinoma: a case report.伴有肾细胞癌的梅耶-罗基坦斯基-库斯特-豪泽综合征：一例报告
J Pediatr Hematol Oncol. 2013 Oct;35(7):e309-10. doi: 10.1097/MPH.0b013e3182707321.
3
Mayer-Rokitansky-Kuster-Hauser syndrome diagnosed by magnetic resonance imaging in a 15-year-old girl.一名15岁女孩通过磁共振成像诊断为梅耶-罗基坦斯基-库斯特-豪泽综合征。
J Pediatr Adolesc Gynecol. 1997 May;10(2):89-92. doi: 10.1016/s1083-3188(97)70058-5.
4
Müllerian anomalies and renal agenesis: autosomal dominant urogenital adysplasia.
J Pediatr. 1984 Jun;104(6):861-4. doi: 10.1016/s0022-3476(84)80481-3.
5
A Case of Mayer-Rokitansky-Küster-Hauser Syndrome with a Fused Pancake-shaped Pelvic Kidney.1例合并融合型薄饼状盆腔肾的迈耶-罗基坦斯基-库斯特-豪泽综合征病例
Adv Biomed Res. 2019 May 27;8:35. doi: 10.4103/abr.abr_97_18. eCollection 2019.
6
[A case of Mayer-Rokitansky syndrome].
Hinyokika Kiyo. 1988 Aug;34(8):1461-7.
7
Mayer Rokitansky Kuster Hauser syndrome with urogenital sinus anomaly.合并泌尿生殖窦异常的迈耶-罗基坦斯基-库斯特-豪泽综合征
J Coll Physicians Surg Pak. 2007 Jan;17(1):57-8.
8
Glioblastoma arising in a patient with Mayer-Rokitansky-Küster-Hauser syndrome.Mayer-Rokitansky-Küster-Hauser 综合征患者的胶质母细胞瘤。
J Clin Neurosci. 2013 Oct;20(10):1464-5. doi: 10.1016/j.jocn.2013.06.002. Epub 2013 Sep 7.
9
A case of Mayer-Rokitansky-Küster-Hauser syndrome in a low-resource tertiary hospital in Douala, Cameroon.喀麦隆杜阿拉一家资源匮乏的三级医院里的一例迈耶-罗基坦斯基-库斯特-豪泽综合征病例。
SAGE Open Med Case Rep. 2019 Feb 13;7:2050313X19830817. doi: 10.1177/2050313X19830817. eCollection 2019.
10
A rare case of 46,XX gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome.一例罕见的46,XX性腺发育不全合并迈耶-罗基坦斯基-库斯特-豪泽综合征。
J Hum Reprod Sci. 2016 Oct-Dec;9(4):263-266. doi: 10.4103/0974-1208.197694.
本文引用的文献
1
Further evidence that the WT1 gene does not have a role in the development of the derivatives of the müllerian duct.进一步证明WT1基因在苗勒管衍生物的发育过程中不起作用。
Am J Obstet Gynecol. 1998 Sep;179(3 Pt 1):597-603. doi: 10.1016/s0002-9378(98)70051-1.
2
Uterus didelphys with unilateral imperforate hemivagina and ipsilateral renal agenesis.双子宫伴单侧阴道闭锁和同侧肾缺如。
J Pediatr Adolesc Gynecol. 1998 Feb;11(1):25-7. doi: 10.1016/s1083-3188(98)70103-2.
3
Vaginal and uterine anomalies in the pediatric and adolescent patient.儿科及青少年患者的阴道和子宫异常
J Pediatr Adolesc Gynecol. 1998 Feb;11(1):3-11. doi: 10.1016/s1083-3188(98)70100-7.
4
Müllerian agenesis: an update.
Obstet Gynecol. 1997 Aug;90(2):307-12. doi: 10.1016/S0029-7844(97)00256-1.
5
Double uterus, blind hemivagina, and ipsilateral renal agenesis: 36 cases and long-term follow-up.双子宫、盲端半阴道及同侧肾缺如：36例病例及长期随访
Obstet Gynecol. 1997 Jul;90(1):26-32. doi: 10.1016/S0029-7844(97)83836-7.
6
Uterus didelphis with obstructed hemivagina and ipsilateral renal agenesis: ultrasound and magnetic resonance imaging diagnosis.双子宫伴梗阻性半阴道及同侧肾缺如：超声与磁共振成像诊断
Gynecol Obstet Invest. 1997;43(3):209-11. doi: 10.1159/000291857.
7
The double uterus associated with an obstructed hemivagina and ipsilateral renal agenesis.
Am J Obstet Gynecol. 1980 Oct 1;138(3):339-42. doi: 10.1016/0002-9378(80)90260-4.
8
[Renal agenesis, bicornuate uterus and cyst of the Gartner's duct].[肾缺如、双角子宫和加特纳管囊肿]
Ann Pediatr (Paris). 1991 May;38(5):341-3.
9
[Mayer-Rokitansky syndrome. Case report].
Minerva Chir. 1992 Jun 30;47(12):1119-23.
10
Familial occurrence of renal and Müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay.肾和苗勒管发育不全、颅面畸形、严重生长发育迟缓的家族性发病情况。
Am J Med Genet. 1992 Oct 1;44(3):293-6. doi: 10.1002/ajmg.1320440306.
Zotero 插件