| Literature DB >> 27761175 |
Matthew T Whitehead1, Guy Helman2, Andrea L Gropman2.
Abstract
Xp21.2 duplication syndrome is a rare genetic disorder of undetermined prevalence and clinical relevance. As the use of chromosomal microarray has become first line for the work-up of childhood developmental delay, more gene deletions and duplications have been recognized. To the best of our knowledge, the imaging findings of Xp21.2 duplication syndrome have not been reported. We report a case of a 33 month-old male referred for developmental delay that was found to have an Xp21.2 duplication containing IL1RAPL1 and multiple midline brain malformations.Entities:
Keywords: Xq21.2 duplication; corpus callosum; fornix; hypothalamus; olfactory; vermis
Mesh:
Year: 2016 PMID: 27761175 PMCID: PMC5065289 DOI: 10.3941/jrcr.v10i5.2563
Source DB: PubMed Journal: J Radiol Case Rep ISSN: 1943-0922