MR Imaging Findings in Xp21.2 Duplication Syndrome
DOI:
https://doi.org/10.3941/jrcr.v10i5.2563Keywords:
Xq21.2 duplication, hypothalamus, corpus callosum, fornix, vermis, olfactoryAbstract
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.
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Published
2016-05-28
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Neuroradiology
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