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Results 1 - 10 of 27 for Hermaphroditism
  1. ... 46,XX or 46,XY can result in disorders of sex development. These include 45,XO (only one X chromosome), ... Donohoue PA. Disorders of sex development. In: Kliegman RM, St. Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, eds. Nelson Textbook of Pediatrics. ...
  2. ... and symptoms of the condition. 46,XX testicular disorder of sex development 46,XX testicular DSD nonsyndromic 46,XX testicular ... male syndrome Genetic Testing Registry: 46,XX testicular disorder of sex development 46,XX testicular disorder of sex development National ...
  3. Androgen insensitivity syndrome is a condition that affects sexual development before birth and during puberty. People with this condition have one X chromosome ...
  4. ... to inability to have children (infertility). 46,XY disorder of sex development due to LH defects LCH Leydig cell agenesis ...
  5. ... signs and symptoms of the condition. 46,XX disorder of sex development (DSD) due to placental aromatase deficiency Estrogen synthetase ...
  6. Cytochrome P450 oxidoreductase deficiency is a disorder of hormone production. This condition specifically affects steroid hormones, which are needed for normal ...
  7. ... pure gonadal dysgenesis Genetic Testing Registry: 46,XY disorder of sex development and 46,XY complete gonadal dysgenesis Genetic Testing ... Exome sequencing for the diagnosis of 46,XY disorders of sex development. J Clin Endocrinol Metab. 2015 Feb;100(2): ...
  8. ... gynecomastia Testosterone 17-beta-dehydrogenase deficiency 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency ...
  9. ... have been identified in people with 46,XY disorder of sex development, also known as partial gonadal dysgenesis. Affected individuals ... problems. NR5A1 gene variants that cause 46,XY disorder of sex development impair the function of steroidogenic factor 1, though ...
  10. ... also been identified in people with 46,XY disorder of sex development, which is also known as partial gonadal dysgenesis. ... Ostrer H. Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in ...
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