Autosomal recessive Noonan-like syndrome caused by homozygosity for a previously unreported variant in SPRED2

Eur J Med Genet. 2023 Feb;66(2):104695. doi: 10.1016/j.ejmg.2023.104695. Epub 2023 Jan 3.

Abstract

Noonan syndrome is characterized by variable phenotypic expressivity with characteristic dysmorphic facial features, varying degrees of intellectual disability, developmental delay, short stature, and congenital heart defects in 50-80%. Other findings include a webbed neck, cryptorchidism, coagulation defects and eye abnormalities. Thus far, Noonan syndrome has mainly been attributed to heterozygous pathogenic variants in 10+ different genes, with the rare exception of cases due to biallelic pathogenic variants in LZTR1. Recently, homozygous loss-of-function variants in SPRED2 have been identified as a cause of a recessive Noonan syndrome-like phenotype. We present the phenotypes of two additional patients with homozygosity for a previously unreported loss-of-function variant in SPRED2, thereby adding relevant clinical information about the recently described Noonan syndrome-like SPRED2-related phenotype.

Keywords: Dysmorphism; Noonan-like syndrome; SPRED2; Whole exome sequencing.

Publication types

  • Case Reports

MeSH terms

  • Heart Defects, Congenital*
  • Heterozygote
  • Homozygote
  • Humans
  • Intellectual Disability* / genetics
  • Male
  • Noonan Syndrome* / genetics
  • Noonan Syndrome* / pathology
  • Phenotype
  • Repressor Proteins / genetics
  • Transcription Factors / genetics

Substances

  • LZTR1 protein, human
  • Repressor Proteins
  • SPRED2 protein, human
  • Transcription Factors