Veterinary Medicine and Science, Volume 8, Issue 3, Page 953-958, May 2022., 2022 Hermaphroditism is a rare congenital disease that is less frequently occurs in dogs. This report provides the clinical, diagnostic, and surgical approaches for the management of the male pseudohermaphroditism case in dogs that are less frequently reported in the veterinary literature. Introduction Hermaphroditism is less frequently reported in dogs and
Hanan Hendawy +6 more
wiley +1 more source
Persistent mullerian duct syndrome in a patient with bilateral cryptorchid testes with seminoma
Journal of Human Reproductive Sciences, 2012 Persistent mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism in which mullerian duct derivatives are present in an otherwise normally differentiated 46 XY male.
Shrinivasan Chamrajan +3 more
doaj +1 more source
Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases
Indian Journal of Urology, 2011 Persistent Mullerian duct syndrome is a rare form of male pseudohermaphroditism, characterized by the presence of the Mullerian duct structures in an otherwise phenotypically as well as genotypically normal male.
Renuka V Inuganti +3 more
doaj +1 more source
Persistent Mullerian Duct Syndrome with Ovarian Endometriosis-A Rare Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2016 Persistent Mullerian Duct Syndrome (PMDS) is a rare form of internal male pseudohermaphroditism, characterised by presence of Mullerian duct derivatives in a genotypic and phenotypic male.
Savitri Mallikarjun Nerune +3 more
doaj +1 more source
Complexities of gender assignment in 17β-hydroxysteroid dehydrogenase type 3 deficiency: is there a role for early orchiectomy? [PDF]
, 2013 BACKGROUND: 17β-Hydroxysteroid dehydrogenase type-3 (17βHSD-3) deficiency is a rare cause of 46,XY disorders of sex development. The enzyme converts androstenedione to testosterone, necessary for masculinization of male genitalia in utero.
Amy Vallerie +6 more
core +1 more source
The Japanese Journal of Urology, 1994 Male pseudohermaphroditism (MPH) is a complex variety of sexual differentiation disorders characterized by deficiency of masculinization of the internal and/or external genital organs in the presence of testicular development as the male gonad. This condition is caused by embryonic failure in the processes of male sexual development, which is a ...
openaire +3 more sources
Normal sex differences in prenatal growth and abnormal prenatal growth retardation associated with 46,XY disorders of sex development are absent in newborns with congenital adrenal hyperplasia due to 21-hydroxylase deficiency [PDF]
, 2011 Background Congenital adrenal hyperplasia due to 21-hydroxylase deficiency is the most common presentation of a disorder of sex development (DSD) in genetic females. A report of prenatal growth retardation in cases of 46,XY DSD, coupled with observations
Laura J Chalmers +5 more
core +2 more sources
Is there a causal association between genotoxicity and the imposex effect? [PDF]
, 2006 There is a growing body of evidence that indicates common environmental pollutants are capable of disrupting reproductive and developmental processes by interfering with the actions of endogenous hormones.
Josephine A. Hagger +13 more
core +2 more sources
Male Pseudohermaphroditism in a non-descript calf [PDF]
Veterinary World, 2008 [Veterinary World 2008; 1(5.000): 148-148]
L.A.Khan,S.G.Utage,H.S.Sontakke,A.R.Shaikh,K.M.Khan,M.M.Qazi and Ziyaullah Siddiqui
doaj
Renal Subcapsular xenografing of human fetal external genital tissue - A new model for investigating urethral development. [PDF]
, 2017 In this paper, we introduce our novel renal subcapsular xenograft model for the study of human penile urethral and clitoral development. We grafted fifteen intact fetal penes and clitorides 8-11 weeks fetal age under the renal capsules of gonadectomized ...
Baskin, Laurence +6 more
core +2 more sources