Differential Diagnosis between Marfan Syndrome and Loeys-Dietz Syndrome Type 4: A Novel Chromosomal Deletion Covering TGFB2.

Stefano Nistri, Rosina De Cario, Elena Sticchi, Gaia Spaziani, Matteo Della Monica, Sabrina Giglio, Silvia Favilli, Betti Giusti, Pierluigi Stefano, Guglielmina Pepe

Journal: Genes 2022;12(10):1462

PMID: 34680857

Abstract

Marfan syndrome (MFS) and Loeys-Dietz syndrome type 4 (LDS4) are two hereditary connective tissue disorders. MFS displays ectopia lentis as a distinguishing, characterising feature, and thoracic aortic ectasia, aneurysm, dissection, and systemic features as manifestations overlapping with LDS4. LDS4 is characterised by the presence of hypertelorism, cleft palate and/or bifid uvula, with possible ectasia or aneurysms in other arteries. The variable age of onset of clinical manifestations makes clinical diagnosis more difficult. In this study, we report the case of a patient with Marfan syndrome diagnosed at our centre at the age of 33 on the basis of typical clinical manifestations of this syndrome. At the age of 38, the appearance of ectasia of the left common iliac artery and tortuosity of the iliac arteries suggested the presence of LDS4. Next Generation Sequencing (NGS) analysis, followed by Array-CGH, allowed the detection of a novel chromosomal deletion including the entire TGFB2 gene, confirming not only the clinical suspicion of LDS4, but also the clinical phenotype associated with the haploinsufficiency mechanism, which is, in turn, associated with the deletion of the entire gene. The same mutation was detected in the two young sons. This emblematic case confirms that we must be very careful in the differential diagnosis of these two pathologies, especially before the age of 40, and that, in young subjects suspected to be affected by MFS in particular, we must verify the diagnosis, extending genetic analysis, when necessary, to the search for chromosomal alterations. Recently, ectopia lentis has been reported in a patient with LDS4, confirming the tight overlap between the two syndromes. An accurate revision of the clinical parameters both characterising and overlapping the two pathologies is highly desirable.

Address: CMSR Veneto Medica-Cardiology Service, 36077 Altavilla Vicentina, Italy.; Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.; Pediatric Cardiology, Azienda Ospedaliera Universitaria Meyer, 50139 Florence, Italy.; Medical Genetics Unit, Cardarelli Hospital, 80131 Napoli, Italy.; Unit of Medical Genetics, Department of Medical Sciences and Public Health, University of Cagliari, 09024 Cagliari, Italy.; Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.; Cardiac Surgery Unit, Careggi Hospital, 50134 Florence, Italy.; Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.; Marfan Syndrome and Related Disorders Regional Referral Center, Careggi Hospital, 50134 Florence, Italy.
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