Affiliation: | 1. https://orcid.org/0000-0003-0714-2469;2. CRB‐BioJel, Institut Jerome Lejeune, France;3. André Mégarbané, MD, PhD, CRB‐BioJel, Institut Jerome Lejeune, 37 rue des Volontaires, Paris, France.;4. Centre for Arab Genomic Studies, Dubai, United Arab Emirates;5. American University of Science and Technology, Faculty of Health Sciences, Lebanon |
Abstract: | We describe a patient with palatal abnormalities—cleft palate and bifid uvula; distinctive facial features—long and triangular face, large ears and nose, thin lips and dental crowding; musculoskeletal abnormalities—severe scoliosis, joint laxity, long digits, flat feet, decreased muscle mass, and diminished muscle strength; and cardiac features—a dilatated ascending aorta at the level of Valsalva sinuses and a patent foramen ovale. Sequence analysis and deletion/duplication testing for a panel of genes involved in connective tissue disorders revealed the presence of a novel homozygous deletion of exons 2–7 in TGFB3 gene. Heterozygous pathogenic mutations in TGFB3 have been associated with Loeys‐Dietz syndrome 5 (LDS5) and Arrhythmogenic Right Ventricular Dysplasia type 1. Here, we report the first case of a homozygous TGFB3 variant associated with a severe LDS5 and Marfan‐like presentation. |