Results 131 to 140 of about 5,457 (170)
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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 ...
F, Davidoff, D D, Federman
openaire +2 more sources
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 ...
F, Davidoff, D D, Federman
openaire +2 more sources
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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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.
openaire +2 more sources
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.
openaire +2 more sources
GONADAL DYSGENESIS AND DIABETES
The Lancet, 1966G, Menzinger, F, Fallucca, D, Andreani
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DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis
Life, 2023Olaf Hiort +2 more
exaly
Wiener Zeitschrift fur innere Medizin und ihre Grenzgebiete, 1998
L, FEHER, G, GYORGY
+8 more sources
L, FEHER, G, GYORGY
+8 more sources
A case report of successful pregnancy in a patient with pure 46,XY gonadal dysgenesis
Fertility and Sterility, 2008Marc A Fritz
exaly

