Reconstrução vaginal pelo retalho neurovascular pudendo crural na síndrome de Rokitansky

Dornelas, Marilho Tadeu; Arruda, Fabrizio Romagnoli de; Sant'Anna, Ludmila Leite; Netto, Gabriel de Mendonça; Machado, Dequitier Carvalho; Corrêa, Marília de Pádua Dornelas; Dornelas, Marcília de Cássia

doi:10.1590/s1983-51752010000300021

Rev. Bras. Cir. Plást. (Impr.)

2010

DOI: 10.1590/s1983-51752010000300021

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Reconstrução vaginal pelo retalho neurovascular pudendo crural na síndrome de Rokitansky

Marilho Tadeu Dornelas¹,

Fabrizio Romagnoli de Arruda²,

Ludmila Leite Sant'Anna³

et al.

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Congenital Absence of Uterus

Anwar¹

2019

GJMS

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These are two case reports of females with primary amenorrhea, well developed secondary sexual characteristics and congenital absence of uterus. The incidence of Mayer-Rokitansky-Kuester-Hauser syndrome was not clearly established, but studies indicate a variation of 1/4,000 and 1/5,000 live births of the female sex. The syndrome is characterized by aplasia of the Müllerian duct (uterus and upper two-thirds of the vagina) on a person who has karyotype 46, XX with female phenotype characteristic of primary amenorrhea in adolescence. Treatment is usually delayed until the patient is ready to begin sexual activity.

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Congenital Absence of Uterus

Anwar¹

2019

GJMS

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Reconstrução vaginal pelo retalho neurovascular pudendo crural na síndrome de Rokitansky

Cited by 1 publication

References 30 publications

Congenital Absence of Uterus

Congenital Absence of Uterus

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