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Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay

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  • Ram Singh
  • Ana S A Cohen
  • Cathryn Poulton
  • Tina Duelund Hjortshøj
  • Moe Akahira-Azuma
  • Geetu Mendiratta
  • Wahab A Khan
  • Dimitar N Azmanov
  • Karen J Woodward
  • Maria Kirchhoff
  • Lisong Shi
  • Lisa Edelmann
  • Gareth Baynam
  • Stuart A Scott
  • Ethylin Wang Jabs
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The ETS2 repressor factor (ERF) is a transcription factor in the RAS-MEK-ERK signal transduction cascade that regulates cell proliferation and differentiation, and pathogenic sequence variants in the ERF gene cause variable craniosynostosis inherited in an autosomal dominant pattern. The reported ERF variants are largely loss-of-function, implying haploinsufficiency as a primary disease mechanism; however, ERF gene deletions have not been reported previously. Here we describe three probands with macrocephaly, craniofacial dysmorphology, and global developmental delay. Clinical genetic testing for fragile X and other relevant sequencing panels were negative; however, chromosomal microarray identified heterozygous deletions (63.7-583.2 kb) on Chromosome 19q13.2 in each proband that together included five genes associated with Mendelian diseases (ATP1A3, ERF, CIC, MEGF8, and LIPE). Parental testing indicated that the aberrations were apparently de novo in two of the probands and were inherited in the one proband with the smallest deletion. Deletion of ERF is consistent with the reported loss-of-function ERF variants, prompting clinical copy-number-variant classifications of likely pathogenic. Moreover, the recent characterization of heterozygous loss-of-function CIC sequence variants as a cause of intellectual disability and neurodevelopmental disorders inherited in an autosomal dominant pattern is also consistent with the developmental delays and intellectual disabilities identified among the two probands with CIC deletions. Taken together, this case series adds to the previously reported patients with ERF and/or CIC sequence variants and supports haploinsufficiency of both genes as a mechanism for a variable syndromic cranial phenotype with developmental delays and intellectual disability inherited in an autosomal dominant pattern.

Original languageEnglish
Article numbera005991
JournalCold Spring Harbor Molecular Case Studies
Volume7
Issue number3
ISSN2373-2873
DOIs
Publication statusPublished - Jun 2021

Bibliographical note

© 2021 Singh et al.; Published by Cold Spring Harbor Laboratory Press.

ID: 67850150