Case of Desbuquois dysplasia type 1: potentially lethal skeletal dysplasia

Pediatr Int. 2014 Aug;56(4):e26-9. doi: 10.1111/ped.12383.

Abstract

We report a boy with Desbuquois dysplasia type 1. He had the typical skeletal changes: a "Swedish key" appearance of the proximal femora; advanced carpal ossification and other distinctive features of the hand, including an extra-ossification center at the base of the proximal phalanx of the index and middle fingers; dislocation of the metacarpophalangeal joint of the index finger; and bifid distal phalanx of the thumb. In addition, he presented with very severe prenatal growth failure, respiratory distress as a neonate, subsequent failure to thrive and susceptibility to airway infection, and sudden death in early childhood. Molecular analysis identified homozygous 1 bp deletion in the Calcium-Activated Nucleotidase 1 gene (CANT1). To our knowledge, this is the first report of Desbuquois dysplasia type 1 in Japan. Our experience suggests potential lethality in the disorder.

Keywords: CANT1 gene; Desbuquois dysplasia; diagnosis; fatal outcome; radiographic characterization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Craniofacial Abnormalities*
  • Dwarfism*
  • Humans
  • Infant, Newborn
  • Joint Instability*
  • Male
  • Ossification, Heterotopic*
  • Polydactyly*

Supplementary concepts

  • Desbuquois syndrome