Download Citation on ResearchGate | Disgenesia gonadal mixta como forma de presentación de un desorden de la diferenciación sexual de causa. Diagnóstico diferencial con disgenesia gonadal mixta | Se presenta el caso de una paciente de 14 años y 8 meses, referida a la consulta por presentar. Title: Disgenesia gonadal mixta: un caso de síndrome de Turner en mosaicismo 45,X/47,XYY. (Spanish); Alternate Title: Mixed gonadal dysgenesis, a case of.
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Please enter User Name Password Error: About MyAccess If your institution subscribes to this resource, and you don’t have a MyAccess Profile, please contact your library’s reference desk for information on how to gain access to this resource from off-campus. Psychomotor development is normal. Magnetic resonance imaging reports uterine hypoplasia, ovaries and discards a pituitary tumor. Detailed information Professionals Summary information Greekpdf Polskipdf.
disgenesia gonadal mixta
In some patients, the possibility of growth hormone treatment needs to be discussed if short stature is found. Accessed December 31, Ginecologia y Obstetricia de Mexico. Infants with male sex assignment may present disgsnesia cryptorchidism, partial testicular dysgenesis, and hypospadias. However, users may print, download, or email articles for individual use.
Clinical description The clinical manifestations are highly variable, ranging from partial virilisation and ambiguous genitalia at birth to patients with a completely male or female phenotype.
Only comments written in English can be processed. Usually, the more dysgenetic gonad needs to be removed. The laparoscopy evaluation revealed central uterus, right testicle and left gonadal streak.
Disgenesia gonadal mixta con fórmula cromosómica 45,X/46,X, (mar). Presentación de una paciente
Sign in via OpenAthens. A year-old woman visits the University Hospital of Santander for a history of primary amenorrhea, normal female appearance, average height and weight for Colombian population, Tanner 3 breasts and external genitalia Tanner 5.
There is no author summary for this article yet. Summary Epidemiology Prevalence is unknown. In patients with male sex assignment, orchidopexy is required for fixation of the testes in the scrotum and biopsy may be recommended at the time of puberty.
Disgenesia gonadal mixta: un caso de síndrome de Turner en mosaicismo 45,X/47,XYY.
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The clinical manifestations are highly variable, ranging from partial virilisation and ambiguous genitalia at birth to patients with a completely male or female phenotype. We report the case of a female infant of 11 motnhs old referred to gynecological pediatric consult of the Instituto Docente de Urologia in Valencia, Carabobo showing genital ambiguity since birth. The uterus is of variable size and the degree of differentiation of the internal genitalia varies.