SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1-mutated patient's management

Clin Genet. 2017 Jul;92(1):99-103. doi: 10.1111/cge.12957. Epub 2017 Feb 22.

Abstract

Steroidogenic factor 1 (encoded by SF1/NR5A1) is a transcription factor with multiple target genes involved in the development and function of multiple steroidogenic and non-steroidogenic tissues. NR5A1 mutations lead to several phenotypes, including sex reversal, spermatogenesis failure, premature ovarian failure and adrenocortical insufficiency. The implication of NR5A1 mutations in spleen development anomalies was recently highlighted. We provide new evidence of this involvement, describing a novel heterozygous non-sense NR5A1 mutation in a 46,XY-DSD with polysplenia female proband and her father, who had hypospadias and asplenia.

Keywords: 46,XY-DSD; SF1; c.1227C>A; spleen development.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adrenal Insufficiency / genetics*
  • Adrenal Insufficiency / pathology
  • Child
  • Female
  • Heterozygote
  • Humans
  • Hypospadias / genetics*
  • Hypospadias / pathology
  • Male
  • Mutation
  • Primary Ovarian Insufficiency / genetics*
  • Primary Ovarian Insufficiency / pathology
  • Sex Determination Processes / genetics
  • Spermatogenesis / genetics
  • Spleen / growth & development
  • Spleen / pathology
  • Steroidogenic Factor 1 / genetics*

Substances

  • NR5A1 protein, human
  • Steroidogenic Factor 1