Genetic screening for fibrillin-1 gene mutations may be used for screening of other family members, including antenatal diagnosis and pre-implantation genetic diagnosis.[3]Tinkle BT, Lacro RV, Burke LW, et al. Health supervision for children and adolescents with Marfan syndrome. Pediatrics. 2023 Apr 1;151(4):e2023061450.
http://www.ncbi.nlm.nih.gov/pubmed/36938616?tool=bestpractice.com
[37]Child AH, Aragon-Martin JA, Sage K. Genetic testing in Marfan syndrome. Br J Hosp Med (Lond). 2016 Jan;77(1):38-41.
http://www.ncbi.nlm.nih.gov/pubmed/26903455?tool=bestpractice.com