A recurrent de novo missense pathogenic variant in SMARCB1 causes severe intellectual disability and choroid plexus hyperplasia with resultant hydrocephalus

Genet Med. 2019 Mar;21(3):572-579. doi: 10.1038/s41436-018-0079-4. Epub 2018 Jun 15.

Abstract

Purpose: SMARCB1 encodes a subunit of the SWI/SNF complex involved in chromatin remodeling. Pathogenic variants (PV) in this gene can give rise to three conditions. Heterozygous loss-of-function germline PV cause rhabdoid tumor predisposition syndrome and schwannomatosis. Missense PV and small in-frame deletions in exons 8 and 9 result in Coffin-Siris syndrome, which is characterized by intellectual disability (ID), coarse facial features, and fifth digit anomalies.

Methods: By a gene matching approach, individuals with a similar SMARCB1 PV were identified. Informed consent was obtained and patient data were collected to further establish genotype-phenotype relationship.

Results: A recurrent de novo missense PV (c.110G>A;p.Arg37His) in exon 2 of SMARCB1, encoding the DNA-binding domain, was identified in four individuals from different genetic centers. They shared a distinct phenotype consisting of profound ID and hydrocephalus due to choroid plexus hyperplasia. Other shared features include severe neonatal feeding difficulties; congenital heart, kidney, and eye anomalies; obstructive sleep apnea; and anemia.

Conclusion: The p.Arg37His PV in the DNA-binding domain of SMARCB1 causes a distinctive syndrome, likely through a gain-of-function or dominant-negative effect, which is characterized by severe ID and hydrocephalus resulting from choroid plexus hyperplasia. This report broadens the phenotypic spectrum associated with PV in SMARCB1.

Keywords: Choroid plexus hyperplasia; Hydrocephalus; Intellectual disability; Recurrent pathogenic variant; SMARCB1.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Choroid Plexus / physiopathology
  • Chromatin Assembly and Disassembly / genetics
  • DNA Helicases / genetics
  • DNA-Binding Proteins / genetics
  • Exome
  • Facies
  • Female
  • Genetic Association Studies
  • Humans
  • Hydrocephalus / genetics*
  • Hyperplasia / genetics
  • Infant
  • Intellectual Disability / genetics*
  • Male
  • Nuclear Proteins / genetics
  • Phenotype
  • SMARCB1 Protein / genetics*
  • SMARCB1 Protein / physiology
  • Transcription Factors / genetics

Substances

  • DNA-Binding Proteins
  • Nuclear Proteins
  • SMARCB1 Protein
  • SMARCB1 protein, human
  • Transcription Factors
  • DNA Helicases