Results 71 to 80 of about 8,371 (167)

Transfer of surgical competences in the treatment of intersex disorders in Togo

open access: yesAfrican Journal of Paediatric Surgery, 2009
Background: To evaluate the impact of scientific seminar on the sexual ambiguity on patients and paediatric surgeons in French-speaking African countries.
Gnassingbe K   +9 more
doaj  

Ovarian cyst in a case of female pseudohermaphroditism in a patient with male phenotype

open access: yes, 2007
Female pseudohermaphroditism is an intersexual state distinguished by virilized external genitals and secondary sex characters in a XX subject. We report a case of female pseudohermaphroditism diagnosed later on the discovery of an abdominal mass, then ...
NIEBEL, THEKLA LARISSA   +8 more
core  

A case of male pseudohermaphroditism with incomplete testicular feminization syndrome [PDF]

open access: yes, 1992
A 19-year-old female visited our hospital because of primary amenorrhea. She was genetically (46XY) male. Her breasts were poorly developed. She had no pubic or axillary hair. The phenotype was female, and the vagina had a short and closed end.
後藤, 毅   +6 more
core  

A case report of female pseudohermaphroditism caused by maternal androluteoma

open access: yes, 2000
Female pseudohermaphroditism is a condition characterized by various degree of external genitalia virilization in a patient with female internal genitalia and karyotype (XX). External genitalia is mascolinized congenitally when female fetus is exposed to
Ferrari F.   +11 more
core  

Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos, and oligohydramnios [PDF]

open access: yes, 2013
ObjectiveTo present female pseudohermaphroditism in a prenatally diagnosed cloacal malformation.Case reportA 29-year-old, primigravid woman referred for counseling at 17 weeks of gestation because of oligohydramnios and an intra-abdominal cyst in the ...
Jun-Wei Su   +7 more
core   +1 more source

Female Pseudohermaphroditism Due To Classical 21-hydroxylase Deficiency In A Girl With Turner Syndrome.

open access: yes, 2015
We report on a rare case of female pseudohermaphroditism due to classical 21-hydroxylase deficiency associated with Turner syndrome (45,X/46,XX). Difficulties in the management of both diseases are briefly discussed.
Matias Baptista, M T   +4 more
core   +1 more source

Male pseudohermaphroditism due to 5-alpha reductase type-2 deficiency in a 20-month old boy

open access: yes, 2016
5-alpha-reductase (5-ARD) type 2 deficiencyis an autosomal sex-linked disorder, resulting inthe inability to convert testosterone to the morephysiological active dihydrotestosterone (DHT).DHT is the most potent androgen, bound selec-tively to the ...
Ida Bagus Andhita, Wayan Bikin Suryawan
core   +1 more source

Persistent müllerian duct syndrome

open access: yesIndian Journal of Pathology and Microbiology, 2009
Persistent Müllerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism characterized by the presence of the Mόllerian duct structures in an otherwise phenotypically as well as genotypically normal male.
Prakash Neeraj   +2 more
doaj  

A Case with late onset of ambiguous genitalia

open access: yesInternational Journal of Reproductive BioMedicine, 2017
Background: Ambiguous genitalia is an uncommon situation that happensbetween 1 and 2 per every 1000 live births and falls under the umbrella diagnosisof disorders of sexual development.
Soraya Saleh Gargari   +3 more
doaj   +2 more sources

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