Warkany Syndrome : A Rare Case Report
Joint Authors
Source
Issue
Vol. 2011, Issue 2011 (31 Dec. 2011), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2011-10-18
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
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.
American Psychological Association (APA)
Agrawal, Amit& Agrawal, Rashmi. 2011. Warkany Syndrome : A Rare Case Report. Case Reports in Pediatrics،Vol. 2011, no. 2011, pp.1-3.
https://search.emarefa.net/detail/BIM-472218
Modern Language Association (MLA)
Agrawal, Amit& Agrawal, Rashmi. Warkany Syndrome : A Rare Case Report. Case Reports in Pediatrics No. 2011 (2011), pp.1-3.
https://search.emarefa.net/detail/BIM-472218
American Medical Association (AMA)
Agrawal, Amit& Agrawal, Rashmi. Warkany Syndrome : A Rare Case Report. Case Reports in Pediatrics. 2011. Vol. 2011, no. 2011, pp.1-3.
https://search.emarefa.net/detail/BIM-472218
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-472218
