Mayer-Rokitansky-Kuster-Hauser syndrome type II: A rare case.
Indian J Hum Genet
;
2013 Jan; 19(1): 113-115
Artigo
em Inglês
| IMSEAR
| ID: sea-147650
ABSTRACT
Mayer-Rokitansky-Kuster-Hauser (MRKH) is a malformation complex comprising absent vagina and absent or rudimentary uterus. MRKH syndrome may be attributed to an initial affection of the intermediate mesoderm consequently leading (by the end of the 4th week of fetal life) to an alteration of the blastema of the cervicothoracicsomites and the pronephricducts. These latter subsequently induce the differentiation of the mesonephric and then the Wolffian and Mullerian ducts. There are very sparse such cases reported. We present a case of type II MRKH or Mullerian renal cervical somite association (i.e., Mullerian duct aplasia, renal dysplasia, and cervical somite anomalies).
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Assunto principal:
Anormalidades Congênitas
/
Anormalidades Múltiplas
/
Feminino
/
Humanos
/
Adulto
/
Síndrome de Dandy-Walker
/
Transtornos 46, XX do Desenvolvimento Sexual
/
Rim
/
Nefropatias
/
Ductos Paramesonéfricos
Idioma:
Inglês
Revista:
Indian J Hum Genet
Ano de publicação:
2013
Tipo de documento:
Artigo
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