HERMAFRODITISMO VERDADEIRO QUIMERA 46,XX/46,XY. Tese apresentada à Universidade Federal de São. Paulo – Escola Paulista de Medicina para a. Título: Hermafroditismo verdadeiro na espécie canina. Título em inglês: True Hermaphroditism in a Dog. Autor(es): Costa, Paula Priscila Correia · Braga Filho . 7 abr. Há três tipos de hermafroditismo: o hermafroditismo verdadeiro, o pseudo- hermafroditismo masculino e o pseudo-hermafroditismo feminino.
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First of all, the inclusion of the karyotype in the name of the disease holds the false premise that the patients do not know the meaning of a 46,XY verdadriro a 46,XX karyotype.
No seu Artigo 4 oafirma-se: Frimberger D, Gearhart JP. Urol Int ; There was a normal size prostate in the pelvic area, exhibiting normal texture and echogenicity. Durval Damiani Rua Bela Cintra verdafeiro, apto. Practical management of the intersex infant.
Genetic counseling Genetic counseling should be offered to families of affected children.
Acta Scientiae Veterinariae
Disorder of sex development; Intersex; Hermaphroditism; Pseudo-hermaphroditism; Gonads; Ambiguous genitalia. Many patients have obvious genital ambiguity and are verdwdeiro at birth. The need for and timing of surgical treatment is complex, depending on sex assignment and gonadal configuration.
Health care resources for this disease Expert centres Diagnostic tests 29 Patient organisations 19 Orphan drug s 0. Other search option s Alphabetical list.
Antes do Consenso, Houk e cols. Definitive diagnosis is based on gonadal histology testicular and ovarian tissue.
Journal of Clinical Investigation 1: No other abnormalities were seen and the owner opted for no further surgical intervention. Anatomical and inherited causes of reproductive failure. Journal of the American Veterinary Medical Association. How to cite this article.
hermafroditismo verdadeiro diagnostico e tratamento
However, ultrasound findings prostate and ovariesand the presence of normal testis and external genitalia without a defined penis or vulva are in accordance with the description of a true hermaphrodite. Some present later with abnormal pubertal development. Abdominal ultrasound was performed to assess presence of sexual glands and gonads. The documents contained in this web site are presented for information purposes only. Clinically, a true hermaphrodite can exhibit different degrees of genital ambiguity; they can be diagnosed during puberty with the emergence of heterosexual characteristics, or as an adult, with infertility or gonadal neoplasia.
Antenatal diagnosis Prenatal diagnosis may be possible following demonstration of atypical genitalia on ultrasound and amniocentesis revealing a 46,XX karyotype. Orchiectomy and slit correction surgery were performed. Testosterone hermafrodltismo explains the male behavior and appearance, demonstrating that the testis were prevalent over the ovaries.
Clinically, verdadeio true hermaphrodite can exhibit different degrees of genital ambiguity; they can be diagnosed during puberty with the emergence of heterosexual characteristics, or as an adult, with infertility or gonadal neoplasia. Cistic ovaries and hyperestrogenism in a canine female pseudohermaphrodite. Show full item record. Patients who present later in life have higher differentiation of genitalia.
Hermaphroditism or intersex is a general term that includes various congenital anomalies of the genital system which is used to define animals with ambiguous sexual characteristics.
How common is intersex? Consensus guidelines recommend referral to a specialist center for examination and treatment.
European Journal of Pediatric. The genetic cause is the absence of the SRY chromosome, which has a verxadeiro role on activation of the SOX gene, which is responsible for sex determination. Diagnostic methods Many patients have obvious genital ambiguity and are diagnosed at birth.
Hermafroditismo verdadeiro na espécie canina | Costa | Acta Scientiae Veterinariae
A prepuce with no apparent function was present cranially to the slit, closer to the umbilical scar. Ovaries were vdrdadeiro on their typical anatomical position; they were symmetrical and had normal sizes.
The exact cause of 46,XX ovotesticular DSD has not been elucidated for the majority of cases but may be related to mosaicism or genetic mutations.