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NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness
Author(s) -
Brown Kerry K.,
Alkuraya Fowzan S.,
Matos Michael,
Robertson Richard L.,
Kimonis Virginia E.,
Morton Cynthia C.
Publication year - 2009
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.32764
Subject(s) - chromosomal inversion , haploinsufficiency , breakpoint , biology , genetics , karyotype , chromosomal rearrangement , chromosome , gene , phenotype
In an effort to discover genes important for human development, we have ascertained patients with congenital anomalies and cytogenetically balanced chromosomal rearrangements. Herein, we report a 4‐year‐old girl with profound deafness, a history of feeding difficulties, dysmorphism, strabismus, developmental delay, and an apparently balanced de novo paracentric chromosome 5 inversion, inv(5)(q15q33.2). Molecular cytogenetic analysis of the inversion revealed the presence of microdeletions of approximately 400–500 kb at or near both breakpoints. The 5q15 microdeletion completely removes the nuclear receptor NR2F1 ( COUP‐TFI ) from the inverted chromosome 5. We propose haploinsufficiency of NR2F1 to be the cause of the patient's deafness and many of the other associated anomalies based on striking similarity with the Nr2f1 null mouse. Additionally, this study further highlights the need for high resolution analysis of clinical samples with chromosomal rearrangements as associated deletions may be primarily responsible for the clinical features of these patients. © 2009 Wiley‐Liss, Inc.