Add to ORKGPuberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hai
17α-hydroxylase and 17,20-lyase are enzymes encoded by the CYP17A1 gene and are required for the syn...
Background: Deficiency of 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) is a rare autosomal rec...
Objective: To review a case of differences of sexual differentiation (DSD) in an adult female patien...
Background: Aromatase deficiency is a rare autosomal recessive disorder. 46,XY-affected patients oft...
A 16-year-old "female" patient presented as hypertension, hypokalemia, male pseudohermaphr...
Association between reproductive factors and urinary estrogens and estrogen metabolites in premenopa...
PubMed ID: 27087292Partial androgen insensitivity syndrome (PAIS) typically presents with micropenis...
Deficiency of 17 beta-hydroxysteroid dehydrogenase type3 (17 beta-HSD3) isoenzyme which catalyzes th...
Constitutional delay of growth and puberty (CDGP) is the most common cause of pubertal delay. CDGP i...
Testicular adrenal rest tumors (TART) occur often as asymptomatic nodules in cortico-tropin-dependen...
17 beta-hydroxysteroid dehydrogenase type 3 deficiency is a rare cause of 46 XY disorders of sexual ...
Context: Hypothalamic kisspeptin signaling plays a critical role in the initiation and maintenance o...
17 alpha-hydroxylase and 17 beta-hydroxylase deficiency are rare causes of 46XY disorders of sexual ...
Aim 17 alpha-hydroxylase enzyme deficiency is a rare form of congenital adrenal hyperplasia (CAH) an...
PubMedID: 20543690Purpose of Review: What controls puberty remains largely unknown and current gene ...
17α-hydroxylase and 17,20-lyase are enzymes encoded by the CYP17A1 gene and are required for the syn...
Background: Deficiency of 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) is a rare autosomal rec...
Objective: To review a case of differences of sexual differentiation (DSD) in an adult female patien...
Background: Aromatase deficiency is a rare autosomal recessive disorder. 46,XY-affected patients oft...
A 16-year-old "female" patient presented as hypertension, hypokalemia, male pseudohermaphr...
Association between reproductive factors and urinary estrogens and estrogen metabolites in premenopa...
PubMed ID: 27087292Partial androgen insensitivity syndrome (PAIS) typically presents with micropenis...
Deficiency of 17 beta-hydroxysteroid dehydrogenase type3 (17 beta-HSD3) isoenzyme which catalyzes th...
Constitutional delay of growth and puberty (CDGP) is the most common cause of pubertal delay. CDGP i...
Testicular adrenal rest tumors (TART) occur often as asymptomatic nodules in cortico-tropin-dependen...
17 beta-hydroxysteroid dehydrogenase type 3 deficiency is a rare cause of 46 XY disorders of sexual ...
Context: Hypothalamic kisspeptin signaling plays a critical role in the initiation and maintenance o...
17 alpha-hydroxylase and 17 beta-hydroxylase deficiency are rare causes of 46XY disorders of sexual ...
Aim 17 alpha-hydroxylase enzyme deficiency is a rare form of congenital adrenal hyperplasia (CAH) an...
PubMedID: 20543690Purpose of Review: What controls puberty remains largely unknown and current gene ...
17α-hydroxylase and 17,20-lyase are enzymes encoded by the CYP17A1 gene and are required for the syn...
Background: Deficiency of 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) is a rare autosomal rec...
Objective: To review a case of differences of sexual differentiation (DSD) in an adult female patien...