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Quoted phrase not found in phrase index: "Persistent mullerian duct syndrome, type I"
Page 1
Surgical management and molecular diagnosis of persistent Mullerian duct syndrome in Chinese patients.
Tian HJ, Wu DH, Ru W, Wu DW, Tao C, Chen GJ, Yuan JN, Fu JF, Tang DX. Tian HJ, et al. Asian J Androl. 2022 Jan-Feb;24(1):78-84. doi: 10.4103/aja202175. Asian J Androl. 2022. PMID: 34810374 Free PMC article.
Persistent Mullerian duct syndrome (PMDS) is a rare clinically and genetically overlapping disorder caused by mutations in the anti-Mullerian hormone (AMH) gene or the anti-Mullerian hormone receptor type 2 (AMHR2) gene. ...All but two patients …
Persistent Mullerian duct syndrome (PMDS) is a rare clinically and genetically overlapping disorder caused by mu …
The possible role of AMH in shortening the gubernacular cord in testicular descent: A reappraisal of the evidence.
Hutson JM, Lopez-Marambio FA. Hutson JM, et al. J Pediatr Surg. 2017 Oct;52(10):1656-1660. doi: 10.1016/j.jpedsurg.2017.05.021. Epub 2017 May 27. J Pediatr Surg. 2017. PMID: 28599968 Review.
In the human with aberrant AMH function, the boy has cryptorchidism with persistent Mullerian duct syndrome (PMDS), where the testes are often intraabdominal and on an abnormally long gubernacular cord. ...The controversy could be resolved by re-examin …
In the human with aberrant AMH function, the boy has cryptorchidism with persistent Mullerian duct syndrome (PMD …
A 27 base-pair deletion of the anti-mullerian type II receptor gene is the most common cause of the persistent mullerian duct syndrome.
Imbeaud S, Belville C, Messika-Zeitoun L, Rey R, di Clemente N, Josso N, Picard JY. Imbeaud S, et al. Hum Mol Genet. 1996 Sep;5(9):1269-77. doi: 10.1093/hmg/5.9.1269. Hum Mol Genet. 1996. PMID: 8872466
The persistent mullerian duct syndrome, characterized by the lack of regression of mullerian derivatives, uterus and tubes in otherwise normally masculinized males, is a genetically transmitted disorder implicating either anti-mullerian hormone (AMH), …
The persistent mullerian duct syndrome, characterized by the lack of regression of mullerian derivatives, uterus …
Insensitivity to anti-müllerian hormone due to a mutation in the human anti-müllerian hormone receptor.
Imbeaud S, Faure E, Lamarre I, Mattéi MG, di Clemente N, Tizard R, Carré-Eusèbe D, Belville C, Tragethon L, Tonkin C, Nelson J, McAuliffe M, Bidart JM, Lababidi A, Josso N, Cate RL, Picard JY. Imbeaud S, et al. Nat Genet. 1995 Dec;11(4):382-8. doi: 10.1038/ng1295-382. Nat Genet. 1995. PMID: 7493017
We have now cloned and mapped the human AMH receptor gene and provide genetic proof that it is required for AMH signalling, by identifying a mutation in the AMH receptor in a patient with persistent Mullerian duct syndrome. The mutation destroys the in …
We have now cloned and mapped the human AMH receptor gene and provide genetic proof that it is required for AMH signalling, by identifying a …
Three novel AMH gene mutations in a patient with persistent mullerian duct syndrome and normal AMH serum dosage.
Menabò S, Balsamo A, Nicoletti A, Gennari M, Pirazzoli P, Cicognani A, Baldazzi L. Menabò S, et al. Horm Res. 2008;70(2):124-8. doi: 10.1159/000137664. Epub 2008 Jun 12. Horm Res. 2008. PMID: 18547961
BACKGROUND: Persistentmullerian duct syndrome (PMDS) is characterized by the presence of uterus, fallopian tubes and the upper part of the vagina in 46,XY patients with perfectly virilized external genitalia. It is mostly caused by mutations of the AMH or AMH type 2 recept …
BACKGROUND: Persistentmullerian duct syndrome (PMDS) is characterized by the presence of uterus, fallopian tubes and the upper part of the v …