A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features.

Mol Syndromol. 2014 Jan;5(1):32-5. Epub 2013 Nov 02

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摘要

We describe a boy presenting with intellectual disability and dysmorphic features in whom a cryptic microdeletion in chromosome band 2q12.1 was identified with array CGH. The deletion results in a loss of the POU3F3 and MRPS9 genes. In this paper, we discuss the possible role of POU3F3 haploinsufficiency in relation to the boy's phenotype.

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A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features.

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