Premium
Delineation of a recognizable phenotype for the recurrent LCR22‐C to D/E atypical 22q11.2 deletion
Author(s) -
BengoaAlonso Amaya,
ArtigasLópez Mercè,
MorenoIgoa María,
Cattalli Claudio,
HernándezCharro Blanca,
RamosArroyo Maria Antonia
Publication year - 2016
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.37614
Subject(s) - haploinsufficiency , microcephaly , phenotype , genetics , biology , tetralogy of fallot , gene , deletion syndrome , medicine , heart disease
The 22q11.2 deletion syndrome is typically caused by haploinsufficiency of a 3 Mb region that extends from LCR22‐A until LCR22‐D, while the recurrent recombination between any of the LCR22‐D to H causes the 22q11.2 distal deletion syndrome. Here, we describe three patients with a de novo atypical ∼1.4 Mb 22q11.2 deletion that involves LCR22‐C to a region beyond D (LCR22‐C to D/E), encompassing the distal portion of the typical deleted region and the proximal portion of the distal deletion. We also review six previous published patients with the same rearrangement and compare their features with those found in patients with overlapping deletions. Patients with LCR22‐C to D/E deletion present a recognizable phenotype characterized by facial dysmorphic features, high frequency of cardiac defects, including conotruncal defects, prematurity, growth restriction, microcephaly, and mild developmental delay. Genotype–phenotype analysis of the patients indicates that CRKL and MAPK1 genes play an important role as causative factors for the main clinical features of the syndrome. In particular, CRKL gene seems to be involved in the occurrence of conotruncal cardiac anomalies, mainly tetralogy of Fallot. © 2016 Wiley Periodicals, Inc.