Multiple Coronary Artery Microfistulas in a Girl with Kleefstra Syndrome

Kleefstra syndrome is characterized by hypotonia, developmental delay, dysmorphic features, congenital heart defects, and so forth. It is caused by 9q34.3 microdeletions or EHMT1 mutations. Herein a 20-month-old girl with Kleefstra syndrome, due to a de novo subterminal deletion, is described. She e...

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Bibliografiske detaljer
Udgivet i:Case Rep Genet
Main Authors: Vargiami, Euthymia, Ververi, Athina, Al-Mutawa, Hamda, Gioula, Georgia, Gerou, Spyridon, Rouvalis, Fotios, Kambouris, Marios, Zafeiriou, Dimitrios I.
Format: Artigo
Sprog:Inglês
Udgivet: Hindawi Publishing Corporation 2016
Fag:
Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4867054/
https://ncbi.nlm.nih.gov/pubmed/27239352
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/3056053
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