Journal Article

The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization system

Burnside, Rachel D., Mikhail, Fady M., Ibrahim, Jennifer, Carroll, Andrew J., Robin, Nathaniel H., Godshalk, Robin, Descartes, Maria D., Rush, Brooke, Rutledge, S. Lane

2014

Overview

Purpose: The five segmental duplications (LCR22-D to -H) at the distal region of chromosome 22 band q11.2 in the region immediately distal to the DiGeorge/velocardiofacial syndrome deleted region have been implicated in the recurrent distal 22q11.2 microdeletions. To date, the distal 22q11.2 microdeletions have been grouped together as a single clinical entity despite the fact that these deletions are variable in size and position depending on the mediating LCR22s. Methods: Here, we report 13 new unrelated patients with variable size deletions in the distal 22q11.2 region as shown by cytogenomic array analyses. We compare our patients’ clinical features with those of previously reported cases to better dissect the phenotypic correlations based on the deletion size and position. Results: Six patients had the 1.1-Mb deletion flanked by LCR22-D and -E, and presented clinically with a phenotype consistent with previously reported cases with distal 22q11.2 microdeletions. Three patients had the 1.8-Mb deletion flanked by LCR22-D and -F, and presented with a similar phenotype. Four patients had the 700-kb deletion flanked by LCR22-E and -F, and presented with a milder phenotype that lacked growth restriction and cardiovascular defects. Conclusion: We suggest that the recurrent distal 22q11.2 microdeletions do not represent a single clinical entity, and propose categorizing these deletions into three types according to their genomic position. All three deletion types are thought to be pathogenic and are most often de novo. They all share some presenting features but also have their unique features and risks. Genet Med 16 1, 92–100.

• Publisher: Nature Publishing Group US
• Subject: 631/208/737 / 692/420/2489 / Abnormalities, Multiple - diagnosis / Abnormalities, Multiple - genetics / Abnormalities, Multiple - pathology / Adolescent / Biomedical and Life Sciences / Biomedicine / Child / Child, Preschool / Chromosome Deletion / Chromosomes, Human, Pair 22 - genetics / Comparative Genomic Hybridization / DiGeorge Syndrome - diagnosis / DiGeorge Syndrome - genetics / DiGeorge Syndrome - pathology / Female / Genetic Variation / Human Genetics / Humans / Laboratory Medicine / Male / original-research-article / Phenotype / Polymorphism, Single Nucleotide / Young Adult