Clinical characterisation of the multiple maternal hypomethylation syndrome in siblings

Research output: Contribution to journalJournal articleResearchpeer-review

  • Susanne E Boonen
  • Sven Pörksen
  • Deborah Jg Mackay
  • Østergaard, Elsebet
  • Birthe Olsen
  • Karen Brøndum-Nielsen
  • I Karen Temple
  • Johanne Md Hahnemann
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.
Original languageEnglish
JournalEuropean Journal of Human Genetics
Volume16
Issue number4
Pages (from-to)453-61
Number of pages8
ISSN1018-4813
DOIs
Publication statusPublished - 2008

Bibliographical note

Keywords: Beckwith-Wiedemann Syndrome; Child, Preschool; Consanguinity; DNA Methylation; Diabetes Mellitus; Fatal Outcome; Female; Genomic Imprinting; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Male; Mothers; Pedigree; Phenotype; Siblings; Syndrome

ID: 10486202