Classification of Brain Magnetic Resonance Imaging Abnormalities and Spectrum of Neurological Findings in a Cohort with Copy Number Variation-Related Disorders

CNV-related disorders should be considered in the differential diagnosis of patients with brain MRI findings suspicious for metabolic disorders. Brain MRI differences in patients with the same chromosomal deletion can be explained by the second-hit hypothesis. Additional single nucleotide variations and epigenetic factors in these cases may have led to the involvement of different regions of the brain. Revealing the phenotypic and genotypic characteristics of cases in rare disorders will contribute to the widespread use of precision medicine and genetic treatment approaches in the near future.

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Publication Details

Journal
Molecular Syndromology
Published
2024-08-23
DOI
https://doi.org/10.1159/000540599
Primary Topic
Genomic variations and chromosomal abnormalities
Type
article
Field-Weighted Citation Impact
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article

Classification of Brain Magnetic Resonance Imaging Abnormalities and Spectrum of Neurological Findings in a Cohort with Copy Number Variation-Related Disorders

Emine Çalışkan, Yasemin Akın, Ayberk Türkyılmaz, Safiye Güneş Sağer et al.
Molecular Syndromology
Genomic variations and chromosomal abnormalities
article

Classification of Brain Magnetic Resonance Imaging Abnormalities and Spectrum of Neurological Findings in a Cohort with Copy Number Variation-Related Disorders

Emine Çalışkan, Yasemin Akın, Ayberk Türkyılmaz, Safiye Güneş Sağer, Merve Akçay, Baran Baytar, Oğuzhan Demir
article en

Abstract

CNV-related disorders should be considered in the differential diagnosis of patients with brain MRI findings suspicious for metabolic disorders. Brain MRI differences in patients with the same chromosomal deletion can be explained by the second-hit hypothesis. Additional single nucleotide variations and epigenetic factors in these cases may have led to the involvement of different regions of the brain. Revealing the phenotypic and genotypic characteristics of cases in rare disorders will contribute to the widespread use of precision medicine and genetic treatment approaches in the near future.

Molecular SyndromologyVol. 16(2)
Karadeniz Technical University (TR)
Good health and well-being
Openalex Percentile: Top 85%
Genomic variations and chromosomal abnormalities
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