1973
DOI: 10.1210/jcem-36-4-634
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Cyclical Ovarian Function in Women with Congenital Absence of the Uterus and Vagina

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Cited by 60 publications
(30 citation statements)
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“…However, it is unlikely to have a similar role in women because it is well established that after hysterectomy (Beavis, Brown & Smith, 1969) and in the congenital absence of Mullerian duct structures (Fallopian tubes, uterus, vagina) the cyclic ovarian function is maintained (Brown, Kellar & Matthew, 1959;Fraser, Baird, Hobson, Michie & Hunter, 1973). This paper has shown clearly that there is a cyclic variation in the levels…”
Section: Discussionmentioning
confidence: 79%
“…However, it is unlikely to have a similar role in women because it is well established that after hysterectomy (Beavis, Brown & Smith, 1969) and in the congenital absence of Mullerian duct structures (Fallopian tubes, uterus, vagina) the cyclic ovarian function is maintained (Brown, Kellar & Matthew, 1959;Fraser, Baird, Hobson, Michie & Hunter, 1973). This paper has shown clearly that there is a cyclic variation in the levels…”
Section: Discussionmentioning
confidence: 79%
“…PGF-2ais now believed to be the uterine luteolytic agent in most species except primates (see Horton & Poyser, 1976, for review). Human luteal function appears to be independent of uterine control since neither hysterectomy (Beling, Marcus & Markham, 1970) nor congenital absence of Fallopian tubes, uterus and vagina (Fraser, Baird, Hobson, Michie & Hunter, 1973) disrupt cyclic ovarian function. PGF-2a in vitro, however, in cultured human granulosa cells (McNatty, Henderson & Sawers, 1975), or directly injected into the human ovary (Korda, Shutt, Smith, Shearman & Lyneham, 1975) reduces progesterone secretion, suggesting a possible intraovarian role for in man.…”
Section: Introductionmentioning
confidence: 99%
“…Mainly in familial cases, MRKH is inherited as an autosomal dominant trait with variable expressivity and incomplete penetrance. 8 In women diagnosed with MRKH syndrome, levels of luteinizing hormone, plasmatic follicle stimulating hormone and 17ß-oestradiol are normal proving the integrity of ovarian function. 9 She had presented with karyotype 46, XX chromosome with normal development of secondary sexual characteristics and normal LH, FSH levels.…”
Section: Case Reportmentioning
confidence: 99%