American journal of medical genetics. Part A · 2021
Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome.
Клинический случайПоддержка NIH: внешняя программаСтатьяНазвание и аннотация: Перевод в очереди
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.
Hildebrandt Clara C, Patel Nisha, Graham John M, Bamshad Michael, Nickerson Deborah A, White Janson J, Marvin Colby T, Miller Danny E, University of Washington Center for Mendelian Genomics, Grand Katheryn L, Sanchez-Lara Pedro A, Schweitzer Daniela, Al-Zaidan Hamad I, Al Masseri Zainab, Alkuraya Fowzan S, Lin Angela E
Аннотация
Van den Ende-Gupta syndrome (VDEGS) is a rare autosomal recessive condition characterized by distinctive facial and skeletal features, and in most affected persons, by biallelic pathogenic variants in SCARF2. We review the type and frequency of the clinical features in 36 reported individuals with features of VDEGS, 15 (42%) of whom had known pathogenic variants in SCARF2, 6 (16%) with negative SCARF2 testing, and 15 (42%) not tested. We also report three new individuals with pathogenic variants in SCARF2 and clinical features of VDEGS. Of the six persons without known pathogenic variants in SCARF2, three remain unsolved despite extensive genetic testing. Three were found to have pathogenic ABL1 variants using whole exome sequencing (WES) or whole genome sequencing (WGS). Their phenotype was consistent with the congenital heart disease and skeletal malformations syndrome (CHDSKM), which has been associated with ABL1 variants. Of the three unsolved cases, two were brothers who underwent WGS and targeted long-range sequencing of both SCARF2 and ABL1, and the third person who underwent WES and RNA sequencing for SCARF2. Because these affected individuals with classical features of VDEGS lacked a detectable pathogenic SCARF2 variant, genetic heterogeneity is likely. Our study shows the importance of performing genetic testing on individuals with the VDEGS "phenotype," either as a targeted gene analysis (SCARF2, ABL1) or WES/WGS. Additionally, individuals with the combination of arachnodactyly and blepharophimosis should undergo echocardiography while awaiting results of molecular testing due to the overlapping physical features of VDEGS and CHDSKM.
Предметные рубрики MeSH
Abnormalities, MultipleAdolescentAdultArachnodactylyBlepharophimosisChildChild, PreschoolContractureFemaleGenes, RecessiveGenetic HeterogeneityGenetic Predisposition to DiseaseHeart Defects, CongenitalHumansInfantMaleMiddle AgedProto-Oncogene Proteins c-ablScavenger Receptors, Class FExome SequencingYoung Adult