ACTH-dependent precocious pseudopuberty in an infant with DAX1 gene mutation

Diego Yeste, Cristina González-Niño, Guiomar Pérez De Nanclares, Gustavo Pérez-Nanclares, Laura Audi, Luis Castaño, Antonio Carrascosa

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13 Citations (Scopus)

Abstract

DAX1 gene (Xp21) expression is involved in the development of the hypothalamo-pituitary-gonadal and adrenal axes, and acts as a negative regulator of steroidogenesis. Mutations of this gene determine adrenal hypoplasia congenita (AHC) and hypogonadotropic hypogonadism. We report the case of a 9-month-old boy referred for the study of macrogenitosomia and pubic hair development. He had presented acute adrenal crises in the neonatal period and, later, a clinical picture of peripheral precocious puberty. A mutation in the DAX1 gene was found (Trp291Arg) and a diagnosis of AHC was made. Replacement doses of hydrocortisone (HC) (10 mg/m2/day) failed to produce a feedback inhibition of adrenocorticotropic hormone (ACTH), and testosterone levels remained high. Testosterone and ACTH values normalized after HC was progressively increased to 18 mg/m2/day. In conclusion, peripheral precocious puberty in patients with DAX1 gene mutations appears to be secondary to the stimulus exerted by ACTH on melanocortin receptors in Leydig cells and to the overexpression of testicular steroidogenesis activators by the loss of transcriptional repression. © 2008 Springer-Verlag.
Original languageEnglish
Pages (from-to)65-69
JournalEuropean Journal of Pediatrics
Volume168
Issue number1
DOIs
Publication statusPublished - 1 Jan 2009

Keywords

  • Adrenal hypoplasia congenita
  • DAX1 gene
  • Infant
  • Peripheral precocious puberty
  • Premature pubarche

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