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Human Genetics

, Volume 80, Issue 1, pp 103–104 | Cite as

Miller-Dieker syndrome and monosomy 17p13:a new case

  • A. Selypes
  • A. László
Clinical Case Reports

Summary

A 12-year-old boy is described with multiple anomalies and a de novo terminal deletion of 17p13. Based on clinical examination, the Miller-Dieker syndrome was diagnosed.

Keywords

Internal Medicine Clinical Examination Metabolic Disease Terminal Deletion Multiple Anomaly 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

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Copyright information

© Springer-Verlag 1988

Authors and Affiliations

  • A. Selypes
    • 1
  • A. László
    • 2
  1. 1.Department of Hygiene and EpidemiologyAlbert Szent-Györgyi Medical UniversitySzegedHungary
  2. 2.Department of PediatricsAlbert Szent-Györgyi Medical UniversitySzegedHungary

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