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3.
Tunisie Medicale [La]. 2002; 80 (6): 356-8
in French | IMEMR | ID: emr-61115

ABSTRACT

We relate one observation about a rare case of genital malformation, where is on association of unilateral hematocopos, bicorn uterine and homolateral renal agenesis. The diagnostic was suspected upon the association with a progressive dysmenorrhe and vaginal mass. Il was confirmed by ethnographie and IRM. The treatment has been conservative and consisted only in the section of the vaginal partition


Subject(s)
Humans , Female , Uterus/abnormalities , Kidney/abnormalities , Vagina/abnormalities , Tomography, X-Ray Computed , Ultrasonography
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