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7p22.2 Microduplication: A Pathogenic CNV?
Bauleo, Alessia; Montesanto, Alberto; Pace, Vincenza; Guarasci, Francesco; Apa, Rosalbina; Brando, Rossella; De Stefano, Laura; Sestito, Simona; Concolino, Daniela; Falcone, Elena.
Afiliação
  • Bauleo A; BIOGENET, Medical and Forensic Genetics Laboratory, 87100 Cosenza, Italy.
  • Montesanto A; Department of Biology, Ecology and Earth Sciences, University of Calabria, 87036 Rende, Italy.
  • Pace V; BIOGENET, Medical and Forensic Genetics Laboratory, 87100 Cosenza, Italy.
  • Guarasci F; BIOGENET, Medical and Forensic Genetics Laboratory, 87100 Cosenza, Italy.
  • Apa R; BIOGENET, Medical and Forensic Genetics Laboratory, 87100 Cosenza, Italy.
  • Brando R; BIOGENET, Medical and Forensic Genetics Laboratory, 87100 Cosenza, Italy.
  • De Stefano L; BIOGENET, Medical and Forensic Genetics Laboratory, 87100 Cosenza, Italy.
  • Sestito S; Pediatric Unit, Department of Science of Health, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
  • Concolino D; Pediatric Unit, Department of Science of Health, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
  • Falcone E; BIOGENET, Medical and Forensic Genetics Laboratory, 87100 Cosenza, Italy.
Genes (Basel) ; 14(6)2023 06 19.
Article em En | MEDLINE | ID: mdl-37372471
Partial duplication of the short arm of chromosome 7 is a rare chromosome rearrangement. The phenotype spectrum associated with this rearrangement is extremely variable even if in the last decade the use of high-resolution microarray technology for the investigation of patients carrying this rearrangement allowed for the identification of the 7p22.1 sub-band causative of this phenotype and to recognize the corresponding 7p22.1 microduplication syndrome. We report two unrelated patients that carry a microduplication involving the 7.22.2 sub-band. Unlike 7p22.1 microduplication carriers, both patients only show a neurodevelopmental disorder without malformations. We better characterized the clinical pictures of these two patients providing insight into the clinical phenotype associated with the microduplication of the 7p22.2 sub-band and support for a possible role of this sub-band in the 7p22 microduplication syndrome.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Deficiência Intelectual Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Deficiência Intelectual Idioma: En Ano de publicação: 2023 Tipo de documento: Article