De novo deletion (14)(q11.2q13) including PAX9: clinical and molecular findings.

@article{Schuffenhauer1999DeND,
  title={De novo deletion (14)(q11.2q13) including PAX9: clinical and molecular findings.},
  author={Simone Schuffenhauer and H J Leifheit and Peter Lichtner and Hartmut Peters and Jan Murken and Patricia Emmerich},
  journal={Journal of medical genetics},
  year={1999},
  volume={36 3},
  pages={233-6}
}
A 3 year old boy with a de novo deletion (14)(q11.2q13) of paternal origin encompassing the region from D14S264 to D14S70 is described. The patient presented with severe psychomotor retardation, bilateral cleft lip/palate, bilateral colobomas of the optic nerves and retinas, agenesis of the corpus callosum, pes calcaneovarus, reduced oesophageal peristalsis, and swallowing difficulties. This is the first reported case of PAX9 hemizygosity in humans. Haploinsufficiency of the PAX9 gene might be… CONTINUE READING