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Christianson syndrome in a patient with an interstitial Xq26.3 deletion

โœ Scribed by Andreas Tzschach; Reinhard Ullmann; Alischo Ahmed; Thomas Martin; Georg Weber; Oliver Decker-Schwering; Fernand Pauly; Mohammed Ghiath Shamdeen; Wolfgang Reith; Barbara Oehl-Jaschkowitz

Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
263 KB
Volume
155
Category
Article
ISSN
1552-4825

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## Abstract Deletion 3p syndrome is associated with characteristic facial features, growth failure, and mental retardation. Typically, individuals with deletion 3p syndrome have terminal deletions that result in loss of material from 3p25 to 3pter. We present a child with a clinical phenotype consi