Craniosynostosis and kidney malformation in a case of Hennekam syndrome

Am J Med Genet. 1995 May 22;57(1):66-8. doi: 10.1002/ajmg.1320570115.

Abstract

Hennekam syndrome is a rare autosomal recessive syndrome which was described for the first time in 1989. Here, we present a girl with intestinal lymphangiectasia, severe lymphedema of limbs, seizures, mild mental retardation, and facial anomalies consistent with the diagnosis of Hennekam syndrome. In addition, she had an ectopic kidney and craniosynostosis of the coronal suture, 2 manifestations not previously reported in this syndrome. While the molecular basis of Hennekam syndrome remains, as yet, unknown, this report illustrates its variable clinical expression.

Publication types

  • Case Reports

MeSH terms

  • Craniosynostoses / genetics*
  • Face / abnormalities
  • Female
  • Genes, Recessive
  • Humans
  • Infant
  • Intellectual Disability / genetics*
  • Kidney / abnormalities*
  • Lymphedema / genetics*
  • Lymphedema / pathology
  • Seizures / pathology
  • Syndrome