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Hormonal and cytogenetic studies in phenotypically female patients with gonadal dysgenesis
Author(s) -
Muechler Eberhard K.,
Cary Donna,
Friedrich Mary Anna,
Doherty Richard A.,
Donaldson Catherine H.,
Bonfiglio Thomas
Publication year - 1981
Publication title -
international journal of gynecology and obstetrics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.895
H-Index - 97
eISSN - 1879-3479
pISSN - 0020-7292
DOI - 10.1016/0020-7292(81)90049-7
Subject(s) - gonadoblastoma , gonadal dysgenesis , karyotype , endocrinology , medicine , estrone , testosterone (patch) , gonad , dysgerminoma , hormone , turner syndrome , y chromosome , estrogen , dihydrotestosterone , biology , chromosome , androgen , ovary , genetics , gene
In 4 cases of gonadal dysgenesis the clinical, hormonal, cytogenetic, and histological findings were correlated. There were 2 patients with 46, XY karyotype, one patient with 45, X Turner's syndrome and one patient with a 46,XX chromosome complement. All patients had streak gonads with ovarian stroma. In one phenotypically female 46,XY individual an involuted gonadoblastoma was found. Her testosterone was four‐fold higher in gonadal vein blood compared to peripheral blood. Cytogenetic analysis of multiple tissues in both cases with the 46,XY karyotype greatly reduced the probability of mosaicism. In the patient with 45,X Turner's syndrome and in the one with 46,XX gonadal dysgenesis only peripheral blood cells were karyotyped and mosaicism was not further excluded by analysis of other tissues. The concentrations of steroid hormones in gonadal vein blood were low. The levels ranged as follows: estrone 41–98 pg/ml, estradiol 18–90 pg/ml, testosterone 37–294 ng/100 ml, dihydrotestosterone 13–22 ng/100 ml, and progesterone 0.3–1.5 ng/ml. It was concluded that gonadal streaks were similarly deficient in biosynthesis of steroid hormones despite different chromosomal complements.