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Craniosynostosis is a feature of CHD7-related CHARGE syndrome.

Chiara De LucaSimonetta PiconeMatteo CassinaSimone MarzialiSilvia MorlinoLetizia CamerotaGianpiero TamburriniMarco CastoriPiermichele PaolilloLeonardo SalviatiFrancesco Brancati
Published in: American journal of medical genetics. Part A (2021)
CHARGE syndrome is a rare genetic multiple-malformation disorder characterized by wide phenotypic variability. It is often caused by heterozygous variants in CHD7 and, more rarely, SEMA3E. Although craniofacial alterations are frequent in this condition, to date craniosynostosis is not considered part of the clinical spectrum. Here, we report bi-coronal craniosynostosis in a newborn affected by CHARGE syndrome caused by the de novo heterozygous c.6157C>T, p.(Arg2053*) CHD7 variant. We found two additional subjects in the literature with different craniosynostoses and distinct CHD7 alterations. The inclusion of CHD7-related CHARGE syndrome in the group of rare causes of syndromic craniosynostoses is proposed.
Keyphrases
  • case report
  • early onset
  • systematic review
  • solar cells
  • machine learning
  • copy number
  • gene expression
  • dna methylation
  • genome wide
  • intellectual disability