A Case of Mayer-Rokitansky-K ster-Hauser(MRKH) Syndrome with Imperforate Anus and Unilateral Renal Agenesis.
- Author:
Tae Hyung KIM
1
;
Jin Hee KIM
;
Soo Yung KIM
Author Information
1. Department of Pediatrics, College of Medicine, Pusan National University, Busan, Korea. suyung@pusan.ac.kr
- Publication Type:Case Report
- Keywords:
Mayer-Rokitansky-K ster-Hauser syndrome;
Imperforate anus;
Renal agenesis
- MeSH:
Anus, Imperforate*;
Female;
Genitalia;
Humans;
Infant, Newborn;
Infant, Premature;
Karyotype;
Ovulation;
Sex Characteristics;
Uterus;
Vagina
- From:Journal of the Korean Society of Pediatric Nephrology
2006;10(2):233-237
- CountryRepublic of Korea
- Language:Korean
-
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.
