| Literature DB >> 31235381 |
Monica H Wojcik1, Katri Thiele2, Carly F Grant3, Katherine Chao4, Julia Goodrich4, Anne O'Donnell-Luria5, Ronald V Lacro6, Wen-Hann Tan7, Pankaj B Agrawal8.
Abstract
We describe an infant with a phenotype typical of early onset Marfan syndrome whose genetic evaluation, including Sanger sequencing and deletion/duplication testing of FBN1 and exome sequencing, was negative. Ultimately, genome sequencing revealed a deletion missed on prior testing, demonstrating the unique utility of genome sequencing for molecular genetic diagnosis.Entities:
Keywords: FBN1; deletion; fibrillin; genetic
Mesh:
Substances:
Year: 2019 PMID: 31235381 PMCID: PMC6765408 DOI: 10.1016/j.jpeds.2019.05.029
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406