Back to Search Start Over

239-kb Microdeletion Spanning KMT2E in a Child with Developmental Delay: Further Delineation of the Phenotype

239-kb Microdeletion Spanning KMT2E in a Child with Developmental Delay: Further Delineation of the Phenotype

Authors :
Anastasios Mitrakos
Maria Tsipi
Joanne Traeger-Synodinos
Maria Tzetis
Konstantinos Varvagiannis
Konstantina Kosma
Source :
Molecular Syndromology. 12:321-326
Publication Year :
2021
Publisher :
S. Karger AG, 2021.

Abstract

Pathogenic KMT2E variants underly O'Donnell-Luria-Rodan syndrome, a recently described neurodevelopmental disorder characterized by global developmental delay, variable degrees of intellectual disability, and subtle facial dysmorphism. Less common findings include autism, seizures, gastrointestinal (GI) problems, and abnormal head circumference. Occurrence of mostly truncating variants as well as the similar phenotype observed in individuals with deletions spanning KMT2E suggest haploinsufficiency of this gene as a common mechanism for the disorder, while a gain-of-function or dominant-negative effect cannot be ruled out for some missense variants. Deletions reported in the literature encompass several additional known or presumed haploinsufficient genes, thus leading to more complex phenotypes. Here, we describe a male with antenatal onset hydronephrosis, hypotonia, global developmental delay, prominent GI symptoms as well as facial dysmorphism. Chromosomal microarray revealed a 239-kb de novo microdeletion spanning KMT2E and LHFPL3. Clinical presentation of our proband, harboring one of the smallest deletions of the region confirms the core features of this disorder, suggests GI symptoms as a prominent finding in affected individuals while expanding the phenotypic spectrum to abnormalities of the urinary tract.

Details

ISSN :
16618777 and 16618769
Volume :
12
Database :
OpenAIRE
Journal :
Molecular Syndromology
Accession number :
edsair.doi...........85b96524f5a75ae34b930305cb36938d
Full Text :
https://doi.org/10.1159/000516635