Results 61 to 70 of about 2,744 (169)
Hormona antimülleriana (AMH) como herramienta diagnóstica en la mujer [PDF]
La hormona antimülleriana (AMH) es producida por el testículo fetal e infantil en altas cantidades y por el testículo adulto y el ovario, en cantidades más moderadas.
Bedecarraz, Patricia +8 more
core +1 more source
Estrogenic and anti-androgenic endocrine disrupting chemicals and their impact on the male reproductive system [PDF]
Endocrine disrupting chemicals (EDCs) are identified for their ability to perturb the homeostasis of endocrine system and hormonal balance. The male reproductive system is under close control of hormones and each change in their concentration and time of
DE FALCO, MARIA +2 more
core +2 more sources
• Serum oestradiol and progesterone levels were evaluated in relation to intraocular pressure in female dogs. • Systemic physiological parameters, particularly body weight and systolic blood pressure, showed positive associations with intraocular pressure. • Progesterone levels were negatively correlated with blood pressure.
Candemir Özcan +2 more
wiley +1 more source
Persistent Mullerian Duct Syndrome in a Post Orchideopexy Patient with Gyanaecomastia and Hypospadias: A Case Report [PDF]
Persistent Mullerian Duct Syndrome (PMDS), a rare form of male pseudohermaphroditism. It is characterized by the persistence of Mullerian duct structures (uterus, fallopian tubes and upper two-thirds of vagina) in otherwise normally virilized males (
Vinay S. Kundargi +5 more
doaj
ABSTRACT Background Androgen insensitivity syndrome (AIS) is an X‐linked recessive genetic disorder caused by mutations in the androgen receptor (AR) gene, leading to androgen resistance and disorders of sex development (DSD) in 46, XY individuals. It is classified into three phenotypes: complete (CAIS), partial (PAIS), and mild (MAIS).
Fangming Wang +3 more
wiley +1 more source
Introduction Persistent Mullerian duct syndrome is a rare form of male pseudo-hermaphroditism characterized by the presence of Mullerian duct structures in an otherwise phenotypically, as well as genotypically, normal man; only a few cases have been ...
Gujar Nishikant N +6 more
doaj +1 more source
ABSTRACT Background Mixed gonadal dysgenesis (MGD) is a rare form of differences in sex development (DSD) typically associated with 45,X/46,XY mosaicism. The phenotypic presentation of MGD varies from atypical genitalia to typical male or female appearances often associated with Turner stigmata.
Dinesh Giri +6 more
wiley +1 more source
Persistent Müllerian duct syndrome (PMDS) is a rare form of internal male pseudohermaphroditism characterized by retention of Müllerian duct derivatives in a phenotypically and karyotypically male patient.
Manisha Mohapatra +1 more
doaj +1 more source
Paraprostaatcyste met urotheliale aflijning bij een hond [PDF]
An infected paraprostatic cyst originating from the prostate parenchyma was diagnosed in a seven-year-old male American Staffordshire terrier with dysuria.
Chiers, Koen +7 more
core +1 more source
ABSTRACT Uterine didelphys, also known as double uterus, is a congenital anomaly of the female reproductive system that can be associated with a significant number of threatening obstetric complications, such as uterine rupture. We report a rare and complex case of an 18‐year‐old primigravida who presented with uterine rupture due to uterine didelphys ...
Asim Ali +7 more
wiley +1 more source

