Literature DB >> 6261996

Testicular function in prepubertal male pseudohermaphroditism.

S Campo, C Moteagudo, G Nicolau, E Pellizzari, A Belgorosky, M Stivel, M Rivarola.   

Abstract

Testicular function was evaluated in forty-one prepubertal patients with male pseudohermaphroditism by determining serum concentrations of progesterone, 17-hydroxyprogesterone, dehydroepiandrosterone, androstenedione, testosterone and dihydrotestosterone before and after stimulation with hCG and, in some instances, ACTH. Testosterone response to hCG was normal in all subjects. In one patient, a 4-year-old boy, a deficiency of 17,20-desmolase activity was diagnosed based on the coexistence of elevated levels of pregnenolone, 17-hydroxypregnenolone, progesterone and 17-hydroxyprogesterone and low levels of dehydroepiandrosterone and androstenedione. In three other patients enzymatic blocks were suspected but not confirmed. Congenital deficiency of enzymes necessary for testosterone biosynthesis is an uncommon aetiology of male pseudohermaphroditism.

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Year:  1981        PMID: 6261996     DOI: 10.1111/j.1365-2265.1981.tb00360.x

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


  6 in total

Review 1.  The syndrome of 17,20 lyase deficiency.

Authors:  Walter L Miller
Journal:  J Clin Endocrinol Metab       Date:  2011-11-09       Impact factor: 5.958

Review 2.  Surgical approach to male pseudohermaphroditism.

Authors:  M G Packer
Journal:  Eur J Pediatr       Date:  1993       Impact factor: 3.183

3.  Partial 17, 20-desmolase and 17 alpha-hydroxylase deficiencies in a 16-year-old boy.

Authors:  D Bosson; R Wolter; M Toppet; J R Franckson; E de Peretti; M G Forest
Journal:  J Endocrinol Invest       Date:  1988 Jul-Aug       Impact factor: 4.256

4.  X-linked congenital adrenal hypoplasia associated with hypospadias in an Egyptian baby: a case report.

Authors:  Kotb Abbass Metwalley; Hekma Saad Farghaly
Journal:  J Med Case Rep       Date:  2012-12-28

5.  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

6.  Cytogenetics and etiology of ambiguous genitalia in 120 pediatric patients.

Authors:  Angham Al-Mutair; M Anwar Iqbal; Nadia Sakati; Abdullah Ashwal
Journal:  Ann Saudi Med       Date:  2004 Sep-Oct       Impact factor: 1.526

  6 in total

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