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家族性持续性苗勒管综合征

Familial persistent Müllerian duct syndrome.

作者信息

Sloan W R, Walsh P C

出版信息

J Urol. 1976 Apr;115(4):459-61. doi: 10.1016/s0022-5347(17)59242-3.

DOI:10.1016/s0022-5347(17)59242-3
PMID:4634
Abstract

Two phenotypically normal pre-adolescent brothers with bilateral undescended testes were found to have bilateral fallopian tubes, a uterus and a vagina that drained into the prostatic utricle. We have documented this condition radiographically for the first time, gained some insight into the pattern of inheritance and made recommendations for surgical management.

摘要

两名青春期前双侧隐睾的表型正常兄弟被发现有双侧输卵管、子宫和阴道,这些结构通向前列腺小囊。我们首次通过影像学记录了这种情况,对其遗传模式有了一些了解,并对手术治疗提出了建议。

相似文献

1
Familial persistent Müllerian duct syndrome.家族性持续性苗勒管综合征
J Urol. 1976 Apr;115(4):459-61. doi: 10.1016/s0022-5347(17)59242-3.
2
Laparoscopic orchidopexy for persistent müllerian duct syndrome.
Pediatr Surg Int. 1997 Sep;12(7):522-5. doi: 10.1007/BF01258717.
3
Laparoscopic removal of Müllerian structures and orchiopexy for persistent Müllerian duct syndrome.
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Persistent Müllerian duct syndrome: a surgical approach.
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Neglected cryptorchidism: delayed recognition of persistent müllerian duct syndrome and subsequent malignant degeneration.隐匿性隐睾症:持续性苗勒管综合征的延迟诊断及随后的恶性变
Urology. 2013 Sep;82(3):511-4. doi: 10.1016/j.urology.2013.05.020. Epub 2013 Jul 19.
6
Persistent müllerian duct syndrome associated with irreducible inguinal hernia, bilateral cryptorchidism and testicular neoplasia: a case report.持续性苗勒管综合征合并不可复性腹股沟疝、双侧隐睾及睾丸肿瘤:1例报告
Acta Chir Belg. 2006 Jan-Feb;106(1):119-20. doi: 10.1080/00015458.2006.11679852.
7
Persistent Müllerian duct structures in cryptorchid male infants: surgical dilemmas.
J Pediatr Surg. 1979 Apr;14(2):128-31. doi: 10.1016/0022-3468(79)90002-2.
8
Persistent müllerian duct syndrome.持续性苗勒管综合征
Arch Gynecol Obstet. 1998;261(2):105-7. doi: 10.1007/s004040050208.
9
Persistent müllerian duct syndrome: report of a case with bilateral cryptorchidism.持续性苗勒管综合征:一例双侧隐睾病例报告。
Int Urol Nephrol. 1995;27(4):431-8. doi: 10.1007/BF02550079.
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Persistent müllerian duct syndrome: a case report.
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引用本文的文献

1
Persistent Müllerian Duct Syndrome with Supernumerary Testicles Due to a Novel Homozygous Variant in the Gene and Literature Review.因基因中一种新的纯合变异导致的持续性苗勒管综合征合并额外睾丸及文献综述
Diagnostics (Basel). 2024 Nov 21;14(23):2621. doi: 10.3390/diagnostics14232621.
2
A rare case report of bilateral recurrent inguinal hernia due to persistent Müllerian duct syndrome treated by transabdominal preperitoneal repair.经腹腹膜前修补术治疗持续性苗勒管综合征所致双侧复发性腹股沟疝的罕见病例报告
Medicine (Baltimore). 2020 Feb;99(7):e19079. doi: 10.1097/MD.0000000000019079.
3
Persistent Mullerian Duct Syndrome: A Single-Center Experience.
持续性苗勒管综合征:单中心经验
J Indian Assoc Pediatr Surg. 2018 Oct-Dec;23(4):203-205. doi: 10.4103/jiaps.JIAPS_61_17.
4
Robot-assisted laparoscopic hysterectomy, gonadal biopsy, and orchiopexies in an infant with persistent mullerian duct syndrome.机器人辅助腹腔镜子宫切除术、性腺活检和隐睾固定术治疗持续性苗勒管发育不全综合征婴儿。
Urology. 2014 Apr;83(4):915-7. doi: 10.1016/j.urology.2013.10.006. Epub 2013 Nov 15.
5
A single base pair mutation encoding a premature stop codon in the MIS type II receptor is responsible for canine persistent Müllerian duct syndrome.编码苗勒管抑制物质II型受体中一个过早终止密码子的单碱基对突变是犬持续性苗勒管综合征的病因。
J Androl. 2009 Jan-Feb;30(1):46-56. doi: 10.2164/jandrol.108.005736. Epub 2008 Aug 21.
6
Laparoscopic orchidopexy for persistent müllerian duct syndrome.
Pediatr Surg Int. 1997 Sep;12(7):522-5. doi: 10.1007/BF01258717.
7
Persistent müllerian duct syndrome: report of a case with bilateral cryptorchidism.持续性苗勒管综合征:一例双侧隐睾病例报告。
Int Urol Nephrol. 1995;27(4):431-8. doi: 10.1007/BF02550079.
8
The persistent müllerian duct syndrome: a rare cause of cryptorchidism.持续性苗勒管综合征:隐睾症的罕见病因。
Eur J Pediatr. 1993;152 Suppl 2:S76-8. doi: 10.1007/BF02125444.
9
On the mechanism of the retention of the Müllerian ducts in the chick embryo incubated at a temperature above normal.关于在高于正常温度下孵化的鸡胚中苗勒氏管保留的机制
Anat Embryol (Berl). 1981;163(3):345-50. doi: 10.1007/BF00315710.
10
Role of gonadal hormones in development of the sexual phenotypes.性腺激素在性表型发育中的作用。
Hum Genet. 1981;58(1):78-84. doi: 10.1007/BF00284153.