A De Novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features

Overview

Journal Mol Syndromol

Date 2014 Feb 20

PMID 24550763

Citations 10

Authors

A Dheedene

M Maes

S Vergult

B Menten

Affiliations

Soon will be listed here.

Abstract

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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