2005
DOI: 10.1097/01.spv.0000170512.56557.3d
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Congenital Anomalies of the Female Urogenital Tract

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Cited by 6 publications
(7 citation statements)
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References 30 publications
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“…In the study conducted by JayatiNath et al 5 the incidence was 0.1% and similar in the study by Rock et al 1,3 by Crook et al 6 Most authors report incidence between 0.1%-3.5 %.…”
Section: Discussionsupporting
confidence: 51%
“…In the study conducted by JayatiNath et al 5 the incidence was 0.1% and similar in the study by Rock et al 1,3 by Crook et al 6 Most authors report incidence between 0.1%-3.5 %.…”
Section: Discussionsupporting
confidence: 51%
“…Pre-operative assessment of the patients included detailed counseling, physical examination, pelvi-abdominal ultrasound, a full hormonal profile and intravenous urography to exclude associated urological anomalies [1,2]. Mechanical bowel preparation was started 48 h before surgery.…”
Section: Methodsmentioning
confidence: 99%
“…The most widely used operation today for creating a neovagina is the use of a split thickness skin graft procedure developed by Abbe, Wharton and McIndoe. However, there is a need for continuous and prolonged dilatation during the contractile phase of healing to prevent constriction of the dissected space between the rectum and bladder [2].…”
mentioning
confidence: 99%
“…A normal uterus is typically absent on rectoabdominal examination. These findings suggest m€ ullerian anomalies and should prompt imaging studies to clarify upper genital tract anatomy and differentiate MRKH from anomalies such as androgen insensitivity syndrome, vaginal atresia, or cervical agenesis (5).…”
Section: Discussionmentioning
confidence: 96%
“…Affected patients (usually having Mayer-RokitanskyKuster-Hauser syndrome [MRKH]) display normal secondary sexual characteristics, with congenital absence of the vagina and variable uterine/cervical hypoplasia/aplasia. Approximately 90% of affected women have some degree of m€ ullerian development, most often bilateral fibromuscular uterine remnants along the pelvic sidewall, with functional endometrium in only 2%-7% of these remnants (3,5,6). Ovarian endocrine and oocyte function is typically normal, and the karyotype is 46,XX (7).…”
mentioning
confidence: 99%