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Intellectual deficit, X-linked - plagiocephaly

Orpha number ORPHA2898
Prevalence of rare diseases <1 / 1 000 000
Inheritance
  • X-linked recessive
Age of onset Neonatal/infancy
ICD 10 code -
MIM number
Synonym(s) Hyde Forster-McCarthy-Berry syndrome

Summary

This syndrome is characterised by severe intellectual deficit, brachycephaly, plagiocephaly, prominent forehead and coarse facial features. It has been described in two males from one family. Two females belonging to the same family displayed moderate intellectual deficit but no craniofacial dysmorphism. *Author: Orphanet (October 2006)*.

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