Aplasia Utero Vaginal
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1. Clinical, genetic and molecular study of Rokitansky-Mayer-Küster-Hauser syndrome and related conditions / Estudo genético-clínico e molecular da síndrome de Rokitansky-Mayer-Küster-Hauser e condições afins
Background: Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, comprising utero-vaginal atresia in otherwise phenotypically normal women with a normal karyotype (46,XX), has an incidence of about 1/5,000 among newborn girls. Anomalies of the genital tract range from upper vaginal atresia to total Müllerian agenesis (congenital absence of the Fallopian tubes,
Publicado em: 2008