Müllerian ducts can form upper parts of normal female reproductive system and any failure in ductal fusion may lead to Müllerian Duct Anomalies (MDA). We present a case of MDA, a uterus dysplasia with no evidence of cervical or upper vaginal tissue. This case illustrates the role of Magnetic Resonance Imaging (MRI) on MDA diagnosis and urges the need for a unified reliable and practical classif...

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...

Materials and methods Three commercial PMDs were first assessed and then compared during barefoot walking: PMDa and PMDb resistive technology, 1sens/cm – were assessed onsite, while PMDc – capacitive technology, 4sens/cm was tested on-the-bench and on-site [1]. The PMDs were aligned on the floor to capture successive at-regimen steps of the left foot of one trained volunteer; 10 complete steps ...

Persistent Mullerian Duct Syndrome is a rare autosomal recessive disease characterized by persistent Mullerian derivative in patients with 46 XY Karyotype and normal virilization .Here we are presenting a case of incidental finding of Persistent Mullerian Duct Remnants in a 58 yr old man during routine hernioplasty.Histological diagnosis was confirmed by Immunohistochemistry

Vaginal development has been a longstanding controversy, which hampers studies on vaginal diseases as well as cervical and uterine diseases. Most concerns center on: why is the vaginal epithelium different from the uterine epithelium; and where does the vagina originate from? It is commonly held that the rodent vagina has a dual origin: the cranial part is derived from the Mullerian duct (Mulle...

Persistent Mullerian duct syndrome (PMDS), a form of male pseudohermaphroditism, is rare. This is a case report of 40-years-old, an otherwise normal male, presenting with Mullerian duct derivatives and transverse testicular ectopia (TTE) in the sac of irreducible recurrent inguinal hernia.

developmental midline perinasal masses in children are rare lesions specifically in association with choristomas. we encountered a 3-year-old boy with epiphora, a striking mass on the nasal bridge and ipsilateral nasal hypoplasia. ct scan imaging showed multiple calcified areas within the tumor in addition to linear defect in frontal bone, hypoplastic left ethmoidal sinus and left nasal cavity,...

Received January 2008 Accepted October 2008 INTRODUCTION Persistent mullerian duct syndrome (PMDS), or hernia uteri inguinale, describes a group of patients with a 46,XY karyotype and normal male external genitalia, but internal mullerian duct structures. Typically, these phenotypic males have unilateral or bilateral undescended testes, bilateral fallopian tubes, a uterus, and an upper vaginal ...

mullerian duct anomalies (mdas) are relatively common disorders that are particularly responsible for obstetrical complications and have a prevalence of about 3%-4% in the general population (1, 2). uterine malformations may result from arrested development of the mullerian ducts, failure of fusion of the mullerian ducts or failure of resorption of the median septum (1, 2).