Persistent müllerian duct syndrome: literature review and own data

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Persistent Müllerian duct syndrome: A case report and review

Persistent Mullerian duct syndrome is a rare form of internal male pseudohermaphroditism, in which Mullerian duct derivatives (uterus and fallopian tubes) are present in a genotypic (46XY) and phenotypic male. Over 150 cases have been reported, mainly from outside the African setting. This article presents an unexpected case encountered in an African setting. Handicaps in the management were un...

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Radiological Findings in Persistent Müllerian Duct Syndrome: Case Report and Review of Literature.

This case involved a 36-year-old adult male who presented with an unusual inguinal hernia in which the uterus and fallopian tubes were identified as contents of the inguinal hernia sac. These findings reflected a rare autosomal recessive developmental syndrome known as PMDS (persistent Müllerian duct syndrome). The diagnosis was established and confirmed via radiological-mainly MRI-investigation.

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Persistent müllerian duct syndrome--a case report.

An eighteen month old phenotypically and genotypically normal male child was admitted with a left inguinal hernia and a right undescended testis. At operation, he was found to have a uterus, bilateral fallopian tubes, and a vagina in the left hernial sac. Bilateral orchidopexies and excision of the persistent Mullerian duct structures were carried out. This rare case of persistent Mullerian duc...

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Bilateral Cryptorchidism, a rare presentation for persistent Müllerian duct syndrome

Persistent Müllerian duct syndrome (PMDS) is a rare, sex-limited, autosomal recessive disorder representing male pseudo-hermaphroditism. It is observed in males with the presence of female reproductive organs such as the uterus, cervix, and bilateral fallopian tubes along with normally developed male reproductive organs. It generally occurs during embryogenesis due to mutation in anti-Müllerian...

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The management of the persistent Müllerian duct syndrome

OBJECTIVES To report the findings and management of patients with persistent Müllerian duct syndrome (PMDS). PATIENTS AND METHODS Nineteen phenotypically male patients (aged 8 months to 27 years) presented with testicular maldescent. All of them had normal male external genitalia. Two of them had had a previous diagnosis of persistent Müllerian structures. All patients were karyotyped, and ha...

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ژورنال

عنوان ژورنال: Clinical Endocrinology and Endocrine Surgery

سال: 2019

ISSN: 2519-2582,1818-1384

DOI: 10.30978/cees-2019-2-77