Literature DB >> 8339744

Endocrine findings in male pseudohermaphroditism.

M Zachmann1.   

Abstract

Recent discoveries in molecular biology have much clarified the regulation and function of steroid converting enzymes. Most progress has been made in the area of cytochromes, which regulate the side chain cleavage of cholesterol (P-450 SCC) and the 17 alpha-hydroxylase- and 17,20-desmolase (or 17,20-lyase) activities (P-450 17 alpha), as well as in 3 beta-hydroxysteroid dehydrogenase. Nevertheless, there are some discrepancies between fundamental knowledge and clinical experience, which are difficult to understand: why is it possible, e.g., that cases with "pure" 17 alpha-hydroxylase or 17,20-desmolase deficiency exist, when there is only one cytochrome regulating both steps? After a brief review of clinical and biochemical findings in the various defects of testosterone biosynthesis, a case is discussed which is of interest in this respect.

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Year:  1993        PMID: 8339744     DOI: 10.1007/bf02125441

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  54 in total

1.  Steroid 17,20-desmolase deficiency: a new cause of male pseudohermaphroditism.

Authors:  M Zachmann; J A Völlmin; W Hamilton; A Prader
Journal:  Clin Endocrinol (Oxf)       Date:  1972-10       Impact factor: 3.478

2.  Familial male pseudohermaphroditism without gynecomastia due to deficient testicular 17-ketosteroid reductase activity.

Authors:  J R Givens; W L Wiser; R L Summitt; I J Kerber; R N Andersen; D E Pittaway; S A Fish
Journal:  N Engl J Med       Date:  1974-10-31       Impact factor: 91.245

3.  17-hydroxylation deficiency in man.

Authors:  E G Biglieri; M A Herron; N Brust
Journal:  J Clin Invest       Date:  1966-12       Impact factor: 14.808

4.  3 beta-hydroxysteroid dehydrogenase deficiency. Follow-up study in a girl with pubertal bone age.

Authors:  M Zachmann; M G Forest; E De Peretti
Journal:  Horm Res       Date:  1979

5.  Male pseudohermaphroditism due to 17,20-desmolase deficiency.

Authors:  F R Kaufman; G Costin; U Goebelsmann; F Z Stanczyk; M Zachmann
Journal:  J Clin Endocrinol Metab       Date:  1983-07       Impact factor: 5.958

6.  Endocrine studies in a pubertal male pseudohermaphrodite with 17-ketosteroid reductase deficiency.

Authors:  R Virdis; P Saenger; B Senior; M I New
Journal:  Acta Endocrinol (Copenh)       Date:  1978-01

7.  Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.

Authors:  M I New
Journal:  J Clin Invest       Date:  1970-10       Impact factor: 14.808

8.  Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase gene.

Authors:  E Rhéaume; J Simard; Y Morel; F Mebarki; M Zachmann; M G Forest; M I New; F Labrie
Journal:  Nat Genet       Date:  1992-07       Impact factor: 38.330

9.  Hypergonadotrophic hypogonadism in an XX female subject due to 17,20 steroid desmolase deficiency.

Authors:  F Larrea; R Lisker; R Bañuelos; J A Bermúdez; J Herrera; V Núñez Rasilla; G Pérez-Palacios
Journal:  Acta Endocrinol (Copenh)       Date:  1983-07

10.  17-ketosteroid reductase deficiency -- plasma steroids and incubation studies with testicular tissue.

Authors:  K von Schnakenburg; F Bidlingmaier; D Engelhardt; O Butenandt; P Unterburger; D Knorr
Journal:  Acta Endocrinol (Copenh)       Date:  1980-07
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