Results 221 to 230 of about 110,162 (292)
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Thyroiditis and Gonadal Dysgenesis
New England Journal of Medicine, 1964THE high incidence of Hashimoto's thyroiditis in females as compared to males has been repeatedly confirmed since the original description of the disease in 19121 in 4 patients, all middle-aged women. The female proponderance is also true for the occurrence of thyroid antibody in several control series,2 , 3 and for the incidence of focal thyroiditis ...
E. Engel, A. P. Forbes, E. D. Williams
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The journal of obstetrics and gynaecology research, 2019
Coexistence of Mayer‐Rokitansky‐Küster‐Hauser syndrome and gonadal dysgenesis is extremely rare, and a case of Mayer‐Rokitansky‐Küster‐Hauser syndrome with a uterine cervix and normal vagina has not been reported.
I. Kisu +5 more
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Coexistence of Mayer‐Rokitansky‐Küster‐Hauser syndrome and gonadal dysgenesis is extremely rare, and a case of Mayer‐Rokitansky‐Küster‐Hauser syndrome with a uterine cervix and normal vagina has not been reported.
I. Kisu +5 more
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Pediatrics, 1973
The syndrome of mixed gonadal dysgenesis (MGD) is characterized by a unilateral testis, usually intra-abdominal, a streak gonad on the contralateral side, and persistent Mullerian structures. The external genitalia are always masculinized to some extent, on occasion achieveing a normal male phenotype: the somatic signs of Turner's syndrome are ...
Daniel D. Federman, Frank Davidoff
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The syndrome of mixed gonadal dysgenesis (MGD) is characterized by a unilateral testis, usually intra-abdominal, a streak gonad on the contralateral side, and persistent Mullerian structures. The external genitalia are always masculinized to some extent, on occasion achieveing a normal male phenotype: the somatic signs of Turner's syndrome are ...
Daniel D. Federman, Frank Davidoff
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Laparoscopic removal of gonads in gonadal dysgenesis
International Journal of Gynecology & Obstetrics, 1995Prophylactic gonadectomy is widely accepted in male pseudohermaphroditism because of the possible malignant conversion of the gonads. Gonadoblastoma or dysgerminoma may occur in the dysgenetic gonads. Laparoscopic gonadectomy has been performed on a patient and is suggested as the optimum mode of management of patients with dysgenetic gonads.
T. Major, A. Borsos, P. Csiszár
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Gonadal Dysgenesis and Its Variants
Pediatric Clinics of North America, 1972In the last decade, developments in human clinical cytogenetics and improved methods of gonadal visualization have resulted in the description of a wide variety of karyotypic and phenotypic variations in association with gonadal dysgenesis. The purpose of this article is to bring into focus the infinite variety of phenotypes seen with rudimentary ...
Phung Thi Tho, Paul G. McDonough
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Journal of Urology, 1979
Mixed gonadal dysgenesis is an intersex syndrome characterized by a unilateral streak gonad, persistent müllerian duct structures and ambiguous genitalia. These patients are chromatin negative and exhibit XO/XY mosaicism. The disorder probably results from a cytogenetic error that occurs early in embryogenesis.
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Mixed gonadal dysgenesis is an intersex syndrome characterized by a unilateral streak gonad, persistent müllerian duct structures and ambiguous genitalia. These patients are chromatin negative and exhibit XO/XY mosaicism. The disorder probably results from a cytogenetic error that occurs early in embryogenesis.
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Carbohydrate tolerance in gonadal dysgenesis
American Journal of Obstetrics and Gynecology, 1979Among 42 patients with GD, one had clinical diabetes and 10 had chemical diabetes (26%) when tested by OGTT. The insulinogenic index was lower in patients with chemical diabetes than in patients with normal OGTT. Among 19 patients with isolated hypogonadotropic hypogonadism, similarly tested, three had chemical diabetes (15%). In a prospective study of
Eugenio Rasio, Jacques Van Campenhout
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XY gonadal dysgenesis in a heifer
Veterinary Record, 1980The anatomical and histological features of the genital tract of a six-year-old Haryana heifer, which had failed to show oestrus, are described. The heifer had a 60 XY karyotype in the leucocyte culture. The external genital organs were absent and a small opening at the ventral perineal border acted as the external urogenital opening.
JM Nigam +4 more
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Skeletal Abnormalities in Gonadal Dysgenesis
Archives of Internal Medicine, 1964Numerous congenital abnormalities have been described in patients with gonadal dysgenesis. 1 Many of these relate to the skeletal system 2 : The frequency with which these are noted varies greatly, and none is pathognomonic of the condition. A review is presented of these abnormalities, and a description is given of other bone changes that have been ...
Joseph Levin, Herbert S. Kupperman
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GONADAL DYSGENESIS IN THREE SISTERS
The Journal of Clinical Endocrinology & Metabolism, 1959ABSTRACT Elevated levels of serum acid phosphatase are recorded in 3 sisters with gonadal dysgenesis. The clinical features included primary amenorrhea occurring in feminine-appearing women who did not show other stigmata of the Bonnevie-Ullrich-Turner syndrome.
A. Sandler, G. A. Elliott, D. Rabinowitz
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