Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome in a Child with Idiopathic Precocious Puberty
Annals of Pediatric Endocrinology & Metabolism
;
: 126-129, 2012.
Artigo
em Coreano
| WPRIM
| ID: wpr-138738
ABSTRACT
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare congenital disorder characterized by the congenital absence or hypoplasia of the uterus and the upper two thirds of the vagina due to mullerian duct malformation during embryogenesis. MRKH syndrome usually presents as primary amenorrhea in adolescence in females showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. For this reason, MRKH syndrome usually remains undiagnosed until primary amenorrhea or difficulty in sexual intercourse occurs. In this study, a case of MRKH syndrome diagnosed in a child with idiopathic precocious puberty is reported.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Puberdade Precoce
/
Coluna Vertebral
/
Útero
/
Vagina
/
Anormalidades Múltiplas
/
Coito
/
Somitos
/
Desenvolvimento Embrionário
/
Cariótipo
/
Amenorreia
Limite:
Adolescente
/
Criança
/
Feminino
/
Humanos
/
Gravidez
Idioma:
Coreano
Revista:
Annals of Pediatric Endocrinology & Metabolism
Ano de publicação:
2012
Tipo de documento:
Artigo
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