Hysterectomy in a Male! Rare Stigma of a Case of Persistent Mullerian Duct Syndrome
نویسندگان
چکیده
منابع مشابه
A rare case of male pseudohermaphroditism-persistent mullerian duct syndrome with transverse testicular ectopia – Case report and review of literature
INTRODUCTION Persistent Mullerian duct syndrome (PMDS) is a rare type of male pseudohermaphroditism. Transverse testicular ectopia (TTE) is characterized by one testis moving to the opposite side and both testes traversing the same inguinal canal. CASE PRESENTATION An 11-month-old boy presented with bilateral cryptorchidism. The left testis was not palpable; the right testis was canalicular w...
متن کاملPersistent Mullerian Duct Syndrome: a rare entity with a rare presentation in need of multidisciplinary management
MAIN FINDINGS A typical male looking adolescent with a legal female gender assignment presented with haematuria. Investigations led to the diagnosis of Persistent Mullerian Duct Syndrome. The condition is indeed a rare entity that needs a multidisciplinar team management. Case hypothesis: A case of Persistent Mullerian Duct Syndrome undiagnosed at birth because karyotyping was defaulted, thus r...
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15 صفحه اولpersistent mullerian duct syndrome in a 71-year-old man, case report
persistent mullerian duct syndrome in a 71-year-old man, case report h. salehi md , m.r. vatani baf md received:27/06/06 sent for revision: 11/10/06 received revised manuscript: 07/02/07 accepted: 12/02/07 background and objective: normal sexual differentiation occurs in the 6th embryonic week and in a normal embryonic life. both wolffian and mullerian ducts are present until the onset of sexua...
متن کاملRe: Persistent Mullerian Duct Syndrome: a rare entity with a rare presentation in need of multidisciplinary management
We would like to make some comments about the article “Persistent mullerian duct syndrome: a rare entity with a rare presentation in need of multidisciplinary management” (1). The authors report a DSD case diagnosed as PMDS and review some clinical aspects of this exceedingly rare syndrome, but some unclear aspects are notable. The patient described seems to be a case of ambiguous genitalia (pr...
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ژورنال
عنوان ژورنال: The Journal of Obstetrics and Gynecology of India
سال: 2018
ISSN: 0971-9202,0975-6434
DOI: 10.1007/s13224-018-1150-4