Evidence map›Paper›PMID 42510884›Full record

ReviewGenes2026

Chromosome 22q11.2 Microduplication Syndrome: A Review of the Literature and 12 New Cases.

Maria Bisba, Eirini Louizou, Spiros Vittas

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Review in Genes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Maria BisbaDepartment of Quality and Vigilance, Vigi-Care, 11525 Athens, Greece.ORCID 0009-0009-1189-4509
Eirini LouizouDepartment of Molecular Genetics, Cardea Medical, 15233 Athens, Greece.ORCID 0009-0000-1326-1574
Spiros VittasDepartment of Molecular Genetics, Cardea Medical, 15233 Athens, Greece.ORCID 0000-0003-2879-6074

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectives22q11.2 microduplication syndrome is a rare genetic disorder characterized by the presence of one or two additional copies of a segment within the 22q11.2 region of chromosome 22. While much of the literature has focused on the deletion variant leading to DiGeorge syndrome, the duplication counterpart has gained increasing attention due to its clinical variability and under-recognition. This review aims to deliver new possibilities to genetic counseling that can be provided in prenatal and postnatal cases as the phenotype of 22q11.2 microduplication carriers cannot be fully predicted.

methodsIn the present study, a total of 12 (5 prenatal and 7 postnatal) cases were diagnosed through array-CGH and combined with 679 (95 prenatal and 584 postnatal) cases reported in the literature. This review summarizes the published evidence available up to April 2025. Data on clinical presentations, genetic findings, diagnostic methodologies, and outcomes were extracted and analyzed.

resultsThe combination of our cases and the reported cases with 22q11.2 microduplication syndrome revealed a broad phenotypic spectrum. Common clinical features include neurodevelopmental disorders, and cardiac anomalies. Importantly, the syndrome exhibits variable expressivity and reduced penetrance, with more than 70% of the findings to be inherited by one of the parents.

conclusions22q11.2 microduplication syndrome presents a heterogeneous clinical picture with variable expressivity and incomplete penetrance, posing challenges in diagnosis and genetic counseling, particularly when predicting prenatal outcomes. Awareness of its diverse manifestations is crucial for clinicians to consider this syndrome in the differential diagnosis and to provide informed counseling.

Indexed as

Chromosome DuplicationDiGeorge SyndromeAbnormalities, MultipleChromosomes, Human, Pair 22Comparative Genomic HybridizationFemaleGenetic CounselingHumansPhenotypePregnancyPrenatal Diagnosis22q11.2 microduplication syndromearray-CGHgenetic counselingincomplete penetrancevariable expressivity

Identifiers

PMID42510884
PMCPMC13410031

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