Clinical, endocrine, and molecular findings in 17β-hydroxysteroid dehydrogenase type 3 deficiency

M. F. Faienza, L. Giordani, M. Delvecchio, Luci Cavallo

Research output: Contribution to journalArticlepeer-review

Abstract

The 17β-hydroxysteroid dehydrogenases (17βHSD) gene family comprises different enzymes involved in the biosynthesis of active steroid hormones. The 17βHSD type 3 (17βHSD3) isoenzyme catalyzes the reductive conversion of the inactive C19-steroid, △ 4-androstenedione (△4. A), into the biologically active androgen, testosterone (T), in the Leydig cells of the testis. It is encoded by the 17β-hydroxysteroid dehydrogenase type 3 (HSD17B3) gene, which maps to chromosome 9q22. Mutations in the HSD17B3 gene are associated with a rare form of 46,XY disorder of sex development referred to as 17βHSD3 deficiency (or as 17-ketosteroid reductase deficiency), due to impaired testicular conversion of △ 4-A into T. 46,XY patients with 17βHSD3 deficiency are usually classified as female at birth, raised as such, but develop secondary male features at puberty. Diagnosis, and consequently early treatment, is difficult because clinical signs from birth until puberty may be mild or absent. Biochemical diagnosis of 17βHSD3 deficiency requires measurement of serum T/△4-A ratio after hCG stimulation test in pre-pubertal subjects, while baseline values seem to be informative in early infancy and adolescence. However, low basal T/ △4-A ratio is not specific for 17βHSD3 deficiency, being sometimes also found in patients with other defects in T synthesis or with Leydig cells hypoplasia. Mutational analysis of the 17HSDB3 gene is useful in confirming the clinical diagnosis of 17JβHSD3 deficiency. This review describes clinical findings, diagnosis, and molecular basis of this rare disease.

Original languageEnglish
Pages (from-to)85-91
Number of pages7
JournalJournal of Endocrinological Investigation
Volume31
Issue number1
Publication statusPublished - Jan 2008

Keywords

  • 17β-hydroxysteroid dehydrogenase type 3 deficiency
  • 17β-hydroxysteroid dehydrogenases
  • Androgens
  • Disorders of sex development
  • Gene mutations

ASJC Scopus subject areas

  • Endocrinology

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