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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The animal exhibited a behavior vervadeiro territory demarcation with urine typically seen in male dogs. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.

Abdominal ultrasound was performed to assess presence of sexual glands and gonads. Other search option s Alphabetical list. How common is intersex?

Vercadeiro J, Warne G. InfancyNeonatal ICD Detailed information Professionals Summary information Polskipdf Russianpdf Review article English Biochemical endocrine investigation, cytogenetic and molecular genetic tests are required. Patients who present later in life have higher differentiation of genitalia.

European Journal of Pediatric. Therefore, the objective of this report is to describe a case of canine hermaphroditism in a dog with male phenotype, as well as the anatomical and hormonal findings, and classification of the hermaphroditism exhibited by the animal studied.

Disorders of sex development have posed a tremendous challenge not only in the diagnosis but also in the treatment, placing the patient, the family members, and the health team in the difficult task of attributing the best sex of rearing for that specific patient.

hermafroditismo verdadeiro diagnostico e tratamento

Physical, behavioral, endocrinologic, and cytogenetic evaluation of two Standard bred racehorses competing as mares with an intersex condition and high postrace serum testosterone concentrations. Intersex and gender assignment: At the other extremity of the slit, on the pubic region, there was a flaccid structure similar to a penis micropenis with no penile bone and no function.

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The pubic area had 2 testicles, each one in a different scrotum, 1 to the right and 1 to the left of the slit.

Definitive diagnosis is based on gonadal histology testicular and ovarian tissue. For all other comments, please send your remarks via contact us. Diagnosis is commonly made during the neonatal period due to atypical genitalia. No other abnormalities were seen and the owner opted for no further surgical intervention.

Prenatal diagnosis may be possible following demonstration of atypical genitalia on ultrasound and amniocentesis revealing a 46,XX karyotype. Other treatments primarily involve hormone replacement. The exact cause of hermafroditidmo ovotesticular DSD has not been elucidated for the majority of cases but may be related to mosaicism or verdadejro mutations.

Development of external genitalia ranges from apparent female to male genitalia with chordee and hypospadias.

There was a normal size prostate in the pelvic vsrdadeiro, exhibiting normal texture and echogenicity. The genetic cause is the absence of the SRY chromosome, which has a fundamental role on hermafrofitismo of the SOX gene, which is responsible for sex determination. The majority arise as de novo mutations. The material is in no way intended to replace professional medical care by a qualified specialist verdadeieo should not be used as a basis for diagnosis or treatment.

At the other extremity of the slit, on the pubic region, there was a flaccid structure similar to a penis micropenis with no penile bone and no function.

Antenatal diagnosis Prenatal diagnosis may be possible following demonstration of atypical genitalia on ultrasound and amniocentesis revealing a 46,XX karyotype.

Hermafroditismo Humano: by Vitor Andrade on Prezi

Recurrence risk depends on the type of genetic alteration found. Disorder of sex development; Intersex; Hermaphroditism; Pseudo-hermaphroditism; Gonads; Ambiguous genitalia. Check this box if you wish to receive a copy of your message. A child hermafrofitismo in the female vsrdadeiro will not understand that her disease holds a “male” karyotype in its name 46,XY DSD.


Adv Pediatr ; Current views on evaluation, management, and gender assignment of the intersex infant. Acta Scientiae Veterinariae, Porto Alegre, v. The occurrence of XX males has been reported.

There was a normal size prostate in the pelvic area, exhibiting normal texture and echogenicity. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

Semin Reprod Med ; A confusing and stigmatizing nomenclature has been employed and the Chicago Consensus tried to minimize the discomfort with modifications of the current terminology.

Hermafroditismo verdadeiro: experiência com 36 casos

BJU Int ; Please use this identifier to cite or link to this item: The substitution of ovotesticular DSD for true hermaphroditism maintains the stigma of the name since ovotesticular is easily perceived as ovarian and testicular tissues.

If, on one hand, the recognition of using terms like intersex and hermaphroditism are stigmatizing, on the other hand, we need terms that are really neutral to not create problems of sexual identification.

Infertility is common in men whereas women have some potential for fertility.

True hermaphrodites are individuals with testicular and ovarian tissues, either combined in one gonad ovotestis or present hermafroditizmo two separate gonads. The assessment and diagnosis of DSD is complex.

Urol Int ; Most affected individuals have female internal genitalia uterus, hemi-uterus or rudimentary uterus. Prognosis Patients usually have normal life expectancy. Hermafrodltismo point in which there is consensus is that the change of the term “intersex” for “disorder of sex development” is highly desirable and eliminates the idea of an “intermediate sex”. A perspective on the approach to the intersex child born with genital ambiguity.