MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1002/ajmg.a.63531

Медицинская библиотека · American journal of medical genetics. Part A · 2024

3q29 duplications: A cohort of 46 patients and a literature review.

Massier Marie, Doco-Fenzy Martine, Egloff Matthieu, Le Guillou Xavier, Le Guyader Gwenaël, Redon Sylvia, Benech Caroline, Le Millier Karine, Uguen Kevin, Ropars Juliette, Sacaze Elise, Audebert-Bellanger Séverine, Apetrei Andreea, Molin Arnaud, Gruchy Nicolas, Vincent-Devulder Aline, Spodenkiewicz Marta, Jacquin Clémence, Loron Gauthier, Thibaud Marie, Delplancq Geoffroy, Brisset Sophie, Lesieur-Sebellin Marion, Malan Valérie, Romana Serge, Rio Marlène, Marlin Sandrine, Amiel Jeanne, Marquet Valentine, Dauriat Benjamin, Moradkhani Kamran, Mercier Sandra, Isidor Bertrand, Arpin Stéphanie, Pujalte Mathilde, Jedraszak Guillaume, Pebrel-Richard Céline, Salaun Gaëlle, Laffargue Fanny, Boudjarane John, Missirian Chantal, Chelloug Nora, Toutain Annick, Chiesa Jean, Keren Boris, Mignot Cyril, Gouy Evan, Jaillard Sylvie, Landais Emilie, Poirsier Céline

СтатьяОбзорПеревод в очереди

Аннотация

Duplications of the 3q29 cytoband are rare chromosomal copy number variations (CNVs) (overlapping or recurrent ~1.6 Mb 3q29 duplications). They have been associated with highly variable neurodevelopmental disorders (NDDs) with various associated features or reported as a susceptibility factor to the development of learning disabilities and neuropsychiatric disorders. The smallest region of overlap and the phenotype of 3q29 duplications remain uncertain. We here report a French cohort of 31 families with a 3q29 duplication identified by chromosomal microarray analysis (CMA), including 14 recurrent 1.6 Mb duplications, eight overlapping duplications (>1 Mb), and nine small duplications (<1 Mb). Additional genetic findings that may be involved in the phenotype were identified in 11 patients. Focusing on apparently isolated 3q29 duplications, patients present mainly mild NDD as suggested by a high rate of learning disabilities in contrast to a low proportion of patients with intellectual disabilities. Although some are de novo, most of the 3q29 duplications are inherited from a parent with a similar mild phenotype. Besides, the study of small 3q29 duplications does not provide evidence for any critical region. Our data suggest that the overlapping and recurrent 3q29 duplications seem to lead to mild NDD and that a severe or syndromic clinical presentation should warrant further genetic analyses.

Для цитирования: Massier Marie, Doco-Fenzy Martine, Egloff Matthieu, Le Guillou Xavier, Le Guyader Gwenaël, Redon Sylvia, Benech Caroline, Le Millier Karine, Uguen Kevin, Ropars Juliette, Sacaze Elise, Audebert-Bellanger Séverine, Apetrei Andreea, Molin Arnaud, Gruchy Nicolas, Vincent-Devulder Aline, Spodenkiewicz Marta, Jacquin Clémence, Loron Gauthier, Thibaud Marie, Delplancq Geoffroy, Brisset Sophie, Lesieur-Sebellin Marion, Malan Valérie, Romana Serge, Rio Marlène, Marlin Sandrine, Amiel Jeanne, Marquet Valentine, Dauriat Benjamin, Moradkhani Kamran, Mercier Sandra, Isidor Bertrand, Arpin Stéphanie, Pujalte Mathilde, Jedraszak Guillaume, Pebrel-Richard Céline, Salaun Gaëlle, Laffargue Fanny, Boudjarane John, Missirian Chantal, Chelloug Nora, Toutain Annick, Chiesa Jean, Keren Boris, Mignot Cyril, Gouy Evan, Jaillard Sylvie, Landais Emilie, Poirsier Céline. 3q29 duplications: A cohort of 46 patients and a literature review.. American journal of medical genetics. Part A. 2024. DOI: 10.1002/ajmg.a.63531.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.