Genetic testing · 1997
PCR assay for screening patients at risk for 22q11.2 deletion.
СтатьяПоддержка исследования: вне правительства СШАПоддержка службы здравоохранения СШАНазвание 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.
Driscoll D A, Emanuel B S, Mitchell L E, Budarf M L
Аннотация
Deletions of 22q11.2 have been detected in the majority of patients with DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes by either cytogenetic analysis, fluorescence in situ hybridization (FISH), or Southern blot hybridization. However, these techniques may not be the most efficient or cost-effective means of screening large numbers of "at-risk" patients. Therefore, we developed a PCR assay to assess a patient's likelihood of having a 22q11.2 deletion based on homozygosity at consecutive markers in the DiGeorge chromosomal region. The sensitivity and specificity of PCR screening were evaluated in a cohort of cardiac patients. We conclude that a PCR-based assay is a reliable and efficient means of identifying which patients are at greatest risk for a 22q11.2 deletion and should have FISH studies to confirm their deletion status.
Предметные рубрики MeSH
Abnormalities, MultipleBase SequenceChromosome DeletionChromosomes, Human, Pair 22Cohort StudiesDNA PrimersDiGeorge SyndromeEvaluation Studies as TopicFaceGenetic TestingHeart Defects, CongenitalHumansIn Situ Hybridization, FluorescencePolymerase Chain ReactionPolymorphism, GeneticSensitivity and SpecificitySyndromeTandem Repeat Sequences