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J Korean Soc Pediatr Nephrol. 2006 Oct;10(2):233-237. Korean. Case Report.
Kim TH , Kim JH , Kim SY .
Department of Pediatrics, College of Medicine, Pusan National University, Busan, Korea.
Department of Pediatrics, Wallace Memorial Baptist Hospital, Korea.

The clinical features of the Mayer-Rokitansky-K ster-Hauser(MRKH) syndrome include normal female secondary sex characteristics, normal genitalia, congenital absence of vagina, rudimentary or bipartite uterus, normal ovarian function and normal ovulation, 46, XX, karyotype, frequent association of renal, skeletal and other congenital anomalies. We experienced a case of a premature infant with MRKH syndrome who had imperforate anus and unilateral renal agenesis.

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