ECO 3D. We find from totally asymtomatic patients up to women with a repro- ductive pernicious forecast or chronic pelvic pain that it disables her to support a normal life. It is very important to distinguish correctly the anatomical malformation that is observed in every case, though in occasions we might not be capable of including it in a concrete group of the classification of the American Society of Reproduction. Reproductive prognosis.
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Main classes have been divided into sub-classes expressing anatomical varieties with clinical significance. Opportune diagnosis and treatment achieve complete improvement of symptoms, adequate reproductive prognosis and avoid major complications such as endometriosis, pelvic adhesions and infertility. ECR Poster Mulleriabas Cervical and vaginal anomalies are classified independently into sub-classes having clinical significance.
Salgado 1M. The purpose of this review is to demonstrate the pathophysiology, clinical manifestations, diagnostic methods and treatment of the obstructed hemivagina and ipsilateral renal anomaly syndrome. Olmos Cantarero 2D. The new system is designed and developed based on i scientific research through critical review of current proposals and preparation of an initial proposal for discussion between the experts, ii consensus measurement among the experts through the use of the DELPHI procedure and iii consensus development by the SC, taking into account the results of the DELPHI procedure and the comments of the experts.
Learning objectives To illustrate and recognize the fundamental characteristics of uterine congenital malformations using high-field MRI. Alarcon 1F. Obstructed hemivagina and ipsilateral renal anomaly syndrome OHVIRAformerly known as the Herlyn-Werner-Wunderlich syndrome, is a rare entity characterized by the presence of a uterus didelphys with an obstructed hemivagina cause by a vaginal septum and the association of a renal anomaly most commonly renal agenesis ipsilateral to the obstruction.
Users should refer to the original published version of the material for the full abstract. The clinical diagnosis is very challenging and requires imaging studies in which ultrasound and MRI play an essential role in the diagnosis, classification and treatment plan.
Occasionally it may be identified after the evaluation of a patient with infertility or recurrent pregnancy loss. Current State Of The Art Personal information Ana Calderwood: This syndrome may remain undiagnosed during childhood and usually becomes symptomatic after menarche, causing obstructive symptoms. Echoscopy for intrauterine pregnancy and gestational age evaluation: Please read the disclaimer for further details.
Abecasis 1F. Background Congenital malformations of the female genital tract have great clinical importance, mainly in patients on reproductive age. The difficulty diagnosis of these congenital anomalies can be solved knowing their maflormaciones distinctive characteristics. Congenital malformations of the female genital tract are common miscellaneous deviations from normal anatomy with health and reproductive consequences. Until now, three systems have been proposed for their categorization but all of them are associated with serious limitations.
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