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Case Reports in Pediatrics
Volume 2011, Article ID 437101, 3 pages
Case Report

Warkany Syndrome: A Rare Case Report

Department of Pediatrics, Chirayu Medical College & Hospital, Near Bairagarh, Bhopal 462030, India

Received 5 July 2011; Accepted 16 August 2011

Academic Editor: H. Horigome

Copyright © 2011 Amit Agrawal and Rashmi Agrawal. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Warkany syndrome 2 or Trisomy 8 mosaicism (T8M) is a well-described, but very rare, chromosomal abnormality. The phenotype is extremely variable ranging from normal individual to severe malformation syndrome and because of this variability, this condition often goes undiagnosed. We report trisomy 8 mosaicism (T8M) in a 3-year-old boy evaluated for facial dysmorphism and delayed development.