Endocrine Abstracts

Background: Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) is defined as aplasia or hypoplasia of the uterus and vagina in female with normal 46,XX karyotype. Isolated congenital absence of the uterus and vagina is classified as MRKHS type 1 (typical form). If it is associated with at least one concomitant congenital malformation that mainly affect the renal and skeletal system, is classified as MRKHS type 2 (atypical form). We report here the cases of MRKH type 2 with i...