m+Medelevator.RU
← Поиск публикаций
Molecular genetics and metabolism · 2024

Impact of genetic and non-genetic factors on phenotypic diversity in NBAS-associated disease.

СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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.

Hammann Nicole, Lenz Dominic, Baric Ivo, Crushell Ellen, Vici Carlo Dionisi, Distelmaier Felix, Feillet Francois, Freisinger Peter, Hempel Maja, Khoreva Anna L, Laass Martin W, Lacassie Yves, Lainka Elke, Larson-Nath Catherine, Li Zhongdie, Lipiński Patryk, Lurz Eberhard, Mégarbané André, Nobre Susana, Olivieri Giorgia, Peters Bianca, Prontera Paolo, Schlieben Lea D, Seroogy Christine M, Sobacchi Cristina, Suzuki Shigeru, Tran Christel, Vockley Jerry, Wang Jian-She, Wagner Matias, Prokisch Holger, Garbade Sven F, Kölker Stefan, Hoffmann Georg F, Staufner Christian

Аннотация

Biallelic pathogenic variants in neuroblastoma-amplified sequence (NBAS) cause a pleiotropic multisystem disorder. Three clinical subgroups have been defined correlating with the localisation of pathogenic variants in the NBAS gene: variants affecting the C-terminal region of NBAS result in SOPH syndrome (short stature, optic atrophy, Pelger-Huët anomaly), variants affecting the Sec 39 domain are associated with infantile liver failure syndrome type 2 (ILFS2) and variants affecting the ß-propeller domain give rise to a combined phenotype. However, there is still unexplained phenotypic diversity across the three subgroups, challenging the current concept of genotype-phenotype correlations in NBAS-associated disease. Therefore, besides examining the genetic influence, we aim to elucidate the potential impact of pre-symptomatic diagnosis, emergency management and other modifying variables on the clinical phenotype. We investigated genotype-phenotype correlations in individuals sharing the same genotypes (n = 30 individuals), and in those sharing the same missense variants with a loss-of-function variant in trans (n = 38 individuals). Effects of a pre-symptomatic diagnosis and emergency management on the severity of acute liver failure (ALF) episodes also were analysed, comparing liver function tests (ALAT, ASAT, INR) and mortality. A strong genotype-phenotype correlation was demonstrated in individuals sharing the same genotype; this was especially true for the ILFS2 subgroup. Genotype-phenotype correlation in patients sharing only one missense variant was still high, though at a lower level. Pre-symptomatic diagnosis in combination with an emergency management protocol leads to a trend of reduced severity of ALF. High genetic impact on clinical phenotype in NBAS-associated disease facilitates monitoring and management of affected patients sharing the same genotype. Pre-symptomatic diagnosis and an emergency management protocol do not prevent ALF but may reduce its clinical severity.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты