Clinical characterisation of the multiple maternal hypomethylation syndrome in siblings

Eur J Hum Genet. 2008 Apr;16(4):453-61. doi: 10.1038/sj.ejhg.5201993. Epub 2008 Jan 16.

Abstract

We present the first clinical report of sibs with the multiple maternal hypomethylation syndrome. Both sisters presented with transient neonatal diabetes mellitus (TNDM). By methylation-specific PCR of bisulphite-treated DNA, we found a mosaic spectrum of hypomethylation at the following maternally methylated loci in both sibs: ZAC (6q24), KCNQ1OT1 (11p15.5), GRB10 (7p11.2-12), PEG3 (19q13), PEG1/MEST (7q32), and NESPAS (20q13). While the older sister has a milder phenotype, the younger one was severely ill and died at 11 months of age. Despite phenotypic differences, the sisters had several manifestations of both TNDM and BWS in common. The family is highly consanguineous, and the parents are first cousins. We suggest that the genetic defect in this family is a novel, most likely autosomal recessive defect of methylation mechanisms, either in the sisters or in their mother, affecting her oocyte imprinting. The recurrence with affected sibs as reported in this family has implications for genetic counselling.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Beckwith-Wiedemann Syndrome / genetics
  • Child, Preschool
  • Consanguinity
  • DNA Methylation*
  • Diabetes Mellitus / genetics*
  • Fatal Outcome
  • Female
  • Genomic Imprinting*
  • Humans
  • Infant
  • Infant, Newborn
  • Infant, Newborn, Diseases / genetics*
  • Male
  • Mothers
  • Pedigree
  • Phenotype
  • Siblings
  • Syndrome