Neonatal teeth in X-linked Opitz (G/BBB) syndrome

Clin Dysmorphol. 2006 Jul;15(3):185-186. doi: 10.1097/01.mcd.0000198931.09330.e8.

Abstract

Two male siblings are described with a clinical and molecular diagnosis of X-linked Opitz (G/BBB) syndrome and the previously unreported feature of neonatal mandibular incisors.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Child, Preschool
  • Cleft Lip / pathology
  • Cleft Palate / pathology
  • Codon, Nonsense / genetics
  • Facies
  • Family Health
  • Female
  • Genetic Diseases, X-Linked / genetics*
  • Genetic Diseases, X-Linked / pathology
  • Humans
  • Hypertelorism / pathology
  • Hypospadias / pathology
  • Incisor / abnormalities*
  • Infant
  • Infant, Newborn
  • Male
  • Microtubule Proteins / genetics
  • Natal Teeth / pathology*
  • Nuclear Proteins / genetics
  • Syndrome
  • Transcription Factors / genetics
  • Ubiquitin-Protein Ligases

Substances

  • Codon, Nonsense
  • Microtubule Proteins
  • Nuclear Proteins
  • Transcription Factors
  • MID1 protein, human
  • Ubiquitin-Protein Ligases