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Distinctive tomographic features of atlantoaxial dislocation in a boy with acromesomelic dysplasia du Pan syndrome.

Abstract
Distinctive tomographic features of atlantoaxial dislocation have been encountered in a child with du Pan syndrome. Three-dimensional computed tomography scan showed agenesis of the odontoid process associated with significant hypoplasia of the left lateral mass of the odontoid. Bidirectional fluorescent DNA sequencing have been used to identify mutations in the complete coding region (exon 1-2) of the cartilage-derived morphogenic protein 1 gene. No mutation was detected in the analysed region. We report what might be a novel variant of acromesomelic du Pan syndrome.
AuthorsAli Al Kaissi, Farid Ben Chehida, Maher Ben Ghachem, Klaus Klaushofer, Franz Grill
JournalClinical dysmorphology (Clin Dysmorphol) Vol. 18 Issue 2 Pg. 122-126 (Apr 2009) ISSN: 1473-5717 [Electronic] England
PMID19449465 (Publication Type: Case Reports, Journal Article)
Topics
  • Atlanto-Axial Joint (abnormalities, diagnostic imaging)
  • Child, Preschool
  • Consanguinity
  • Humans
  • Lower Extremity Deformities, Congenital (diagnostic imaging, pathology)
  • Male
  • Osteochondrodysplasias (diagnostic imaging, pathology)
  • Radiography

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