Gonadal mosaicism as a rare cause of autosomal recessive inheritance

Clin Genet. 2014 Mar;85(3):278-81. doi: 10.1111/cge.12156. Epub 2013 Apr 22.

Abstract

Autosomal recessive diseases are typically caused by the biparental inheritance of familial mutant alleles. Unusual mechanisms by which the recessiveness of a mutant allele is unmasked include uniparental isodisomy and the occurrence of a de novo chromosomal rearrangement that disrupts the other allele. Gonadal mosaicism is a condition in which a postfertilization mutation is confined to the gamete precursors and is not detected in somatic tissues. Gonadal mosaicism is known to give the impression of autosomal recessive inheritance when recurrence of an autosomal-dominant condition among offspring of phenotypically normal parents is observed. Here, we report an extremely rare event in which maternal gonadal mosaicism for a recessive mutation in COL4A4 caused the recurrence of Alport syndrome within a consanguineous family. Such rare occurrence should be taken into account when analyzing pedigrees both for clinical and research purposes.

Keywords: Alport; COL4A4; autosomal recessive; consanguinity; gonadal mosaicism.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Child, Preschool
  • Collagen Type IV / genetics
  • Consanguinity
  • Exome
  • Female
  • Genes, Recessive*
  • Germ-Line Mutation
  • Gonads / metabolism*
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Male
  • Mosaicism*
  • Mutation
  • Nephritis, Hereditary / diagnosis
  • Nephritis, Hereditary / genetics
  • Pedigree

Substances

  • COL4A4 protein, human
  • Collagen Type IV