Steding, Catherine
Loeys-Dietz syndrome caused by 1q41 deletion including TGFβ2 is associated with a neurodevelopmental phenotype
Tucker, M. E., Lyons, M. J., Demo, E., Wilkes, M. J., Fry, D., MacCarrick, G., Fleischer, J., Thomas, M. J., Groepper, D., and Steding, Catherine
Loeys-Dietz syndrome (LDS) is a connective tissue disorder that commonly results in a dilated aorta, aneurysms, joint laxity, craniosynostosis, and soft skin that bruises easily. Neurodevelopmental abnormalities are uncommon in...
Article
Work1
Article1
Steding, Catherine[remove]1
Demo, E.1
Fleischer, J.1
Fry, D.1
Groepper, D.1
1q41 deletion1
Loeys-Dietz syndrome1
TGFB21
developmental delay1
genetic testing1
English1
Wiley1
20221
Faculty Publications and Research - MUCOM1
Marian University1