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A patient with Phelan‐McDermid syndrome and dilation of the great vessels

We present a patient with Phelan‐McDermid syndrome, a rare neurodevelopmental disorder caused by a 22q13 deletion, with the previously undescribed finding of progressive dilation of the great arteries. While congenital heart defects have been identified in patients previously, dilation of the great...

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書目詳細資料
發表在:Clin Case Rep
Main Authors: Deibert, Emily, Crenshaw, Melissa, Miller, Michelle S.
格式: Artigo
語言:Inglês
出版: John Wiley and Sons Inc. 2019
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6452459/
https://ncbi.nlm.nih.gov/pubmed/30997046
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.2003
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