Literature DB >> 160294

Testicular function in post pubertal male pseudohermaphroditism.

S Campo, M Stivel, G Nicolau, C Monteagudo, M Rivarola.   

Abstract

Testicular endocrine function was studied in twelve post pubertal patients with male pseudohermaphroditism and 46 XY chromosomal constitution. Patients were divided into three groups, four subjects who became feminized during puberty, five who became masculinized during puberty and three who were castrated before puberty. Serum dehydroepiandrosterone, progesterone, 17-hydroxyprogesterone, androstendione, testosterone, dihydrotestosterone, LH and FSH were determined by radioimmunoassay. Patients of the first group had the clinical characteristics of testicular feminization secondary to absence of the androgen receptor. One of the five patients of the second group had deficient testosterone secretion but no enzymatic defect could be demonstrated. One of the subjects castrated before puberty had a deficiency in 17,20-desmolase. Therefore, evidence of a failure of the fetal testes could be found in only two of the twelve patients studied.

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Year:  1979        PMID: 160294     DOI: 10.1111/j.1365-2265.1979.tb03100.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  2 in total

1.  A missense mutation in the human cytochrome b5 gene causes 46,XY disorder of sex development due to true isolated 17,20 lyase deficiency.

Authors:  Jan Idkowiak; Tabitha Randell; Vivek Dhir; Pushpa Patel; Cedric H L Shackleton; Norman F Taylor; Nils Krone; Wiebke Arlt
Journal:  J Clin Endocrinol Metab       Date:  2011-12-14       Impact factor: 5.958

2.  Complete androgen insensitivity syndrome: a rare case of disorder of sex development.

Authors:  Alfonsa Pizzo; Antonio Simone Laganà; Irene Borrielli; Nella Dugo
Journal:  Case Rep Obstet Gynecol       Date:  2013-02-27
  2 in total

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