Results 261 to 270 of about 104,321 (292)
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Incomplete Gonadal Dysgenesis

Urologia Internationalis, 1996
A 21-year-old phenotypic male with ambiguous external genitalia and hypospadias was referred for cytogenetic studies. Exploratory laparotomy revealed presence of a small atropic uterus, unilateral gonadal dysgenesis with fallopian tubes on both sides and a cryptorchid testis on the left side. No gonad could be traced on the right side.
F J, Sheth   +5 more
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Primary gonadal failure

Best Practice & Research Clinical Endocrinology & Metabolism, 2019
The term primary gonadal failure encompasses not only testicular insufficiency in 46,XY males and ovarian insufficiency in 46,XX females, but also those disorders of sex development (DSD) which result in gender assignment that is at variance with the genotype and gonadal type.
Asmahane, Ladjouze, Malcolm, Donaldson
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Splenic-Gonadal fusion

Journal of Pediatric Surgery, 1978
A case of the continuous type of splenic-gonadal fusion in association with phocomelia is ...
H F, Given, E J, Guiney
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MIXED GONADAL DYSGENESIS

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
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Male gonadal dysfunction

Clinics in Endocrinology and Metabolism, 1974
Normal testicular function confers upon the adult male two important attributes, virility and fertility, representing the separate functions of the Leydig or interstitial cells and of the germinal epithelium respectively. The purpose of this chapter is to provide an outline and some details of the clinical and laboratory investigations commonly used in
H W, Baker, B, Hudson
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MIXED GONADAL DYSGENESIS

Acta Endocrinologica, 1975
Mixed gonadal dysgenesis (MCG) is a rare intersexual disorder, characterized in most cases by the presence of a testis and a contralateral streak gonad; in some cases the contralateral gonad may be rudimentary not having differentiated into an ovary or into a testis and in other cases it may be absent.
W, Zäh, A E, Kalderon, J R, Tucci
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Familial gonadal dysgenesis

American Journal of Obstetrics and Gynecology, 1970
A case study of gonadal dysgenesis in 3 sisters is presented. The subjects were examined because of failure of the menarche sexual infantilism deafness and speech defects. All had positive buccal smears and a normal 46:XX karyotype. Vaginal cytology revealed a castrate type of specimen. Streak gonads were found upon laparotomy.
B, Perez-Ballester   +2 more
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Mixed Gonadal Dysgenesi

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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Splenic-gonadal fusion

Urology, 1973
Abstract A case of splenic-gonadal fusion is presented with a review of the salient features of this condition as reported in the literature.
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Selective Gonadal Venography

Radiology, 1969
Selective venography has become a routine diagnostic procedure. Adrenal venography for the definition of masses and for hormone analysis has proved valuable. Recently gonadal venography has been used in the evaluation of varicocele and infertility (1, 3, 4) and Delorme et al. recently catheterized the left gonadal vein (5). It was our intention in this
openaire   +2 more sources

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