Hanhart syndrome

Genet Couns. 2010;21(4):359-62.


We report on a male infant with Hanhart Syndrome. It is classified in "oromandibular limb hypogenesis syndromes" which are a group of rare conditions involving congenital malformations of tongue, mandible, and limbs.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple* / diagnostic imaging
  • Craniofacial Abnormalities* / diagnostic imaging
  • Fatal Outcome
  • Humans
  • Infant, Newborn
  • Limb Deformities, Congenital* / diagnostic imaging
  • Male
  • Radiography
  • Tongue / abnormalities

Supplementary concepts

  • Hanhart syndrome