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Trigonocephaly - short stature - developmental delay

Orpha number ORPHA3369
Prevalence of rare diseases <1 / 1 000 000
Inheritance
  • Unknown
Age of onset No data available
ICD 10 code -
MIM number
Synonym(s) Say-Meyer syndrome

Summary

This syndrome is characterised by short stature, trigonocephaly and developmental delay. It has been described in three males. Moderate intellectual deficit was reported in one of the males and the other two patients displayed psychomotor retardation. X-linked transmission has been suggested but autosomal recessive inheritance can not be ruled out. *Author: Orphanet (October 2006)*.

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