J Korean Soc Pediatr Nephrol.
2006 Oct;10(2):233-237.
A Case of Mayer-Rokitansky-K ster-Hauser(MRKH) Syndrome with Imperforate Anus and Unilateral Renal Agenesis
- Affiliations
-
- 1Department of Pediatrics, College of Medicine, Pusan National University, Busan, Korea. suyung@pusan.ac.kr
- 2Department of Pediatrics, Wallace Memorial Baptist Hospital, Korea.
Abstract
- 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.
- Full Text Links
-
- Actions
-
Cited
- CITED
-
- Close
- Share
-
- Similar articles
-
- A Case of Mayer-Rokitansky-K ster-Hauser Syndrome combined with Unilateral Renal Agenesis and Pelvic Cystic Mass in Child
- A Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome with Amenorrhea and Sexual Precosity
- A Case of Neurogenic Bladder Combined with Mayer-Rokitansky- K ster-Hauser Syndrome
- A Case of Colon Cancer in Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome with Gonadal Agenesis
- A Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome with Bilateral Gonadal Agenesis
