Crossed polydactyly and Greig cephalopolysyndactyly syndrome

Indian Pediatr. 2013 Oct;50(10):967-8. doi: 10.1007/s13312-013-0240-8.

Abstract

Greig cephalopolysyndactyly syndrome is a rare genetic disorder, with an autosomal dominant inheritance and consisting of a triad of polysyndactyly, macrocephaly and hypertelorism. Crossed polydactyly is a finding characteristically associated with this syndrome. We report a one and half year old male child who presented with classic clinical features and family history diagnostic of the above syndrome.

Publication types

  • Case Reports

MeSH terms

  • Acrocephalosyndactylia / diagnosis*
  • Humans
  • Infant
  • Male
  • Polydactyly / diagnosis*
  • Toes / pathology

Supplementary concepts

  • Greig cephalopolysyndactyly syndrome