NPJ genomic medicine · 2021
Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
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.
Sangermano Riccardo, Deitch Iris, Peter Virginie G, Ba-Abbad Rola, Place Emily M, Zampaglione Erin, Wagner Naomi E, Fulton Anne B, Coutinho-Santos Luisa, Rosin Boris, Dunet Vincent, AlTalbishi Ala'a, Banin Eyal, Sousa Ana Berta, Neves Mariana, Larson Anna, Quinodoz Mathieu, Michaelides Michel, Ben-Yosef Tamar, Pierce Eric A, Rivolta Carlo, Webster Andrew R, Arno Gavin, Sharon Dror, Huckfeldt Rachel M, Bujakowska Kinga M
Аннотация
Pathogenic variants in INPP5E cause Joubert syndrome (JBTS), a ciliopathy with retinal involvement. However, despite sporadic cases in large cohort sequencing studies, a clear association with non-syndromic inherited retinal degenerations (IRDs) has not been made. We validate this association by reporting 16 non-syndromic IRD patients from ten families with bi-allelic mutations in INPP5E. Additional two patients showed early onset IRD with limited JBTS features. Detailed phenotypic description for all probands is presented. We report 14 rare INPP5E variants, 12 of which have not been reported in previous studies. We present tertiary protein modeling and analyze all INPP5E variants for deleteriousness and phenotypic correlation. We observe that the combined impact of INPP5E variants in JBTS and non-syndromic IRD patients does not reveal a clear genotype-phenotype correlation, suggesting the involvement of genetic modifiers. Our study cements the wide phenotypic spectrum of INPP5E disease, adding proof that sequence defects in this gene can lead to early-onset non-syndromic IRD.