Oto-onycho-peroneal syndrome: further delineation and first fetal report

Am J Med Genet A. 2004 Jul 30;128A(3):316-9. doi: 10.1002/ajmg.a.30119.

Abstract

We report on the sixth case and first fetal description of oto-onycho-peroneal syndrome (MIM 259780). This entity consists in the association of ear anomalies (-oto), hypoplastic nails (-onycho), hypoplastic or absent fibulae (-peroneal), and shoulder anomalies. Described for the first time by Leiba et al. [1975: Birth Defects 11:67-73] in a male patient, coined by Pfeiffer [1982: Eur J Pediatr 138:317-320], and confirmed by Devriendt et al. [1998: J Med Genet 35:508-509] this condition is most likely autosomal recessive, given the occurrence in sibs of both sexes with normal parents.

MeSH terms

  • Abnormalities, Multiple / diagnosis*
  • Abnormalities, Multiple / diagnostic imaging
  • Abnormalities, Multiple / genetics
  • Adult
  • Ear / abnormalities*
  • Female
  • Fetus / abnormalities*
  • Fibula / abnormalities*
  • Genes, Recessive / genetics
  • Humans
  • Male
  • Nails, Malformed*
  • Pregnancy
  • Shoulder / abnormalities
  • Syndrome
  • Ultrasonography