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Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders. | LitMetric

AI Article Synopsis

Article Abstract

Purpose: To identify genetic etiologies and genotype/phenotype associations for unsolved ocular congenital cranial dysinnervation disorders (oCCDDs).

Methods: We coupled phenotyping with exome or genome sequencing of 467 pedigrees with genetically unsolved oCCDDs, integrating analyses of pedigrees, human and animal model phenotypes, and variants to identify rare candidate single nucleotide variants, insertion/deletions, and structural variants disrupting protein-coding regions. Prioritized variants were classified for pathogenicity and evaluated for genotype/phenotype correlations.

Results: Analyses elucidated phenotypic subgroups, identified pathogenic/likely pathogenic variant(s) in 43/467 probands (9.2%), and prioritized variants of uncertain significance in 70/467 additional probands (15.0%). These included known and novel variants in established oCCDD genes, genes associated with syndromes that sometimes include oCCDDs (e.g., genes that fit the syndromic component of the phenotype but had no prior oCCDD association (e.g., ), genes with no reported association with oCCDDs or the syndromic phenotypes (e.g., ), and genes associated with oCCDD phenocopies that had resulted in misdiagnoses.

Conclusion: This study suggests that unsolved oCCDDs are clinically and genetically heterogeneous disorders often overlapping other Mendelian conditions and nominates many candidates for future replication and functional studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10996726PMC
http://dx.doi.org/10.1101/2024.03.22.24304594DOI Listing

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