Overlap between EEC and AEC syndrome and immunodeficiency in a preterm infant with a TP63 variant

Abstract

<p>Pathogenic variants in the transcription factor <em>TP63 </em>gene cause a variety of clinical phenotypes, such as ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome and ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome. Historically, <em>TP63</em>-related phenotypes have been divided into several syndromes based on both the clinical presentation and location of the pathogenic variant on the <em>TP63</em> gene. This division is complicated by significant overlap between syndromes. Here we describe a patient with clinical characteristics of different <em>TP63</em>-associated syndromes (cleft lip and palate, split feet, ectropion, erosions of the skin and corneas), associated with a de novo heterozygous pathogenic variant c.1681 T>C, p.(Cys561Arg) in exon 13 of the <em>TP63</em> gene. Our patient also developed enlargement of the left-sided cardiac compartments and secondary mitral insufficiency, which is a novel finding, and immune deficiency, which has only rarely been reported. The clinical course was further complicated by prematurity and very low birth weight. We illustrate the overlapping features of EEC and AEC syndrome and multidisciplinary care needed to address the various clinical challenges.</p>