BGDB Sexual Differentiation - Abnormalities: Difference between revisions
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==Additional Information== | ==Additional Information== | ||
* '''Cryptorchidism''' in common eutherian mammals.<ref><pubmed>17379650</pubmed></ref>- [http://www.reproduction-online.org/content/133/3/541/F8.large.jpg Species comparison of descent timeline] | |||
Cryptorchidism in common eutherian mammals.<ref><pubmed>17379650</pubmed></ref>- [http://www.reproduction-online.org/content/133/3/541/F8.large.jpg Species comparison of descent timeline] | * '''Mayer-Rokitansky syndrome''' (MRK anomaly, Rokitansky-Küster-Hauser syndrome, RKH syndrome, RKH) congenital absence of the vagina, dyspareunia, vaginal agenesis. | ||
==References== | ==References== | ||
Revision as of 19:39, 29 Mayıs 2011
| Practical 12: Sex Determination | Early Embryo | Late Embryo | Fetal | Postnatal | Abnormalities | 2011 Audio |
Reproductive Abnormalities
Gonadal Descent
External Genitalia
Hypospadia most common penis abnormality (1 in 300) from a failure of male urogenital folds to fuse in various regions and resulting in a proximally displaced urethral meatus. The cause is unknown, but suggested to involve many factors either indivdually or in combination including: familial inheritance, low birth weight, assisted reproductive technology, advanced maternal age, paternal subfertility and endocrine-disrupting chemicals. Infants with hypospadias should not undergo circumcision.
Opening of the urethra (meatus) on the inferior surface (ring) not at the tip. Other regions where urethra may open to the surface (dashed line).
Hypospadias is classified by the location of the opening
Glandular hypospadias is when external urethral opening is on ventral surface of glans penis. Penile hypospadias is when external urethral opening is on ventral surface of body of the penis. Penoscrotal hypospadias is when external urethral opening is at the junction of penis and scrotum. Perineal hypospadias is when external urethral opening is located on the unfused halves of the scrotum. Epispadias - Uncommon abnormality associated with the penis, 1 in 30,000 infant males, external urethral opening on the dorsal surface of penis.
Internal Genitalia
Male
Ductus Deferens
Unilateral or bilateral absence congenital unilateral absence of the vas deferens (CUAVD), Congenital bilateral absence of the vas deferens (CBAVD) failure of mesonephric duct to differentiate frequent cause of obstructive azoospermia 75% of men with bilateral absence have at least one detectable common mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene
Female
A range of uterine and vaginal anatomical anomalies based upon the abnormal development and fusion of the paramesonephric ducts and vaginal plate development.
Uterine Duplication (uterus didelphys, double uterus, uterus didelphis) A rare uterine developmental abnormality where the paramesonephric ducts (Mullerian ducts) completely fail to fuse generating two separate uterus parts each connected to the cervix and having an ovary each. Failure of fusion of lower paramesonephric ducts, with either double or single vagina.
Septate Uterus
Unicornate Uterus - failure of the paramesonephric ducts to fuse. A single paramesomnephric duct has fused with the vaginal plate and now opens into the vagina, while the other forms a diverticulum.
Cervical: cervical agenesis, cervical duplication
Vagina Absence - Failure of sinovaginal bulb development to form plate, 1 in 4,000 to 5,000 female births.
Environmental Abnormalities
DES Diethylstilbestrol or diethylstilbetrol, is a drug that was prescribed to women from 1938-1971 to prevent miscarriage in high-risk pregnancies. The drug acted as a potent estrogen (mimics natural hormone) and therefore could also act as a potential endocrine disruptor. This led to a number of developing fetal reproductive tract and other abnormalities. In the female fetus, it increased risk of abnormal reproductive tract and also carcinogenic (cancer forming). In the male fetus, it increased the occurance of abnormal genitalia. The drug was banned by FDA (USA) in 1979 as a teratogen, it had previously also been used as livestock growth promoter and could have potentially entered the human food chain. (More? Endocrine Abnormalities | Abnormal Development - Drugs)
| Practical 12: Sex Determination | Early Embryo | Late Embryo | Fetal | Postnatal | Abnormalities | 2011 Audio |
Additional Information
- Cryptorchidism in common eutherian mammals.[1]- Species comparison of descent timeline
- Mayer-Rokitansky syndrome (MRK anomaly, Rokitansky-Küster-Hauser syndrome, RKH syndrome, RKH) congenital absence of the vagina, dyspareunia, vaginal agenesis.
References
- ↑ <pubmed>17379650</pubmed>
BGDB: Lecture - Gastrointestinal System | Practical - Gastrointestinal System | Lecture - Face and Ear | Practical - Face and Ear | Lecture - Endocrine | Lecture - Sexual Differentiation | Practical - Sexual Differentiation | Tutorial
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Cite this page: Hill, M.A. (2026, November 15) Embryology BGDB Sexual Differentiation - Abnormalities. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/BGDB_Sexual_Differentiation_-_Abnormalities
- © Dr Mark Hill 2026, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G