Cardiovascular Manifestations in the Larsen Syndrome

Author:

Kiel Ernest A.1,Frias Jaime L.1,Victorica Benjamin E.1

Affiliation:

1. From the Divisions of Cardiology and Genetics, Department of Pediatrics, University of Florida College of Medicine Gainesville

Abstract

The Larsen syndrome consists of a skeletal dysplasia with multiple joint dislocations and a characteristic facies. The basis of the abnormalities is felt to be a generalized mesenchymal disorder involving connective tissues. More than 80 cases have been reported in the literature with isolated reports of congenital cardiac septal defects and acquired abnormalities of the aorta and mitral valve. A case with marked aortic dilation and insufficiency as well as an aneurysm of the ductus arteriosus is presented. The aortic lesions are similar to those described in other connective tissue disorders, particularly the Marfan syndrome. Previous reports of ductal aneurysms have not revealed an association with connective tissue disorders, but have described a significant morbidity. In summary, patients with the Larsen syndrome are likely to have cardiac lesions similar to those classically associated with the Marfan syndrome; these patients deserve a careful investigation for cardiac anomalies. These aortic lesions may be as prognostically significant as cardiac lesions in the Marfan syndrome.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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1. The health-care utilization and economic burden in patients with genetic skeletal disorders;Orphanet Journal of Rare Diseases;2024-03-04

2. FKBP14kyphoscoliotic Ehlers–Danlos syndrome misdiagnosed as Larsen syndrome: a case report;Molecular Case Studies;2023-06

3. Severe Aortic Root Dilatation in a Patient With Larsen Syndrome;World Journal for Pediatric and Congenital Heart Surgery;2023-03-08

4. Larsen Syndrome;Orthopaedics for the Newborn and Young Child;2023

5. Extending the spectrum in aortopathy: stenosis to aneurysm;Current Opinion in Genetics & Development;2022-10

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