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Ring Chromosome 17 Not Involving the Miller-Dieker Region: A Case with Drug-Resistant Epilepsy

journal contribution
posted on 2023-07-26, 15:04 authored by Antonietta Coppola, Deborah Morrogh, Fiona Farrell, Simona Balestrini, Laura Hernandez-Hernandez, S. Krithika, Josemir W. Sander, Jonathan J. Waters, Sanjay M. Sisodiya
Chromosomal abnormalities are often identified in people with neurodevelopmental disorders including intellectual disability, autism, and epilepsy. Ring chromosomes, which usually involve gene copy number loss, are formed by fusion of subtelomeric or telomeric chromosomal regions. Some ring chromosomes, including ring 14, 17, and 20, are strongly associated with seizure disorders. We report an individual with a ring chromosome 17, r(17)(p13.3q25.3), with a terminal 17q25.3 deletion and no short arm copy number loss, and with a phenotype characterized by intellectual disability and drug-resistant epilepsy, including a propensity for nonconvulsive status epilepticus.

History

Refereed

  • Yes

Volume

9

Issue number

1

Page range

38-44

Publication title

Molecular Syndromology

ISSN

1661-8777

Publisher

Karger Publishers

Language

  • other

Legacy posted date

2020-07-30

Legacy Faculty/School/Department

ARCHIVED Faculty of Science & Technology (until September 2018)

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