A three-year-old boy with the diagnosis of Ehlers-Danlos syndrome (EDS) with persistent ductus arteriosus and multiple diffuse arterial aneurysms is pre sented. The case is classified as "EDS type unknown" because the clinical fea tures and the inheritance pattern differ from the types described previously. It is stressed that the diagnosis of the disease is important for genetic counseling and surgical intervention.
Get full access to this article
View all access options for this article.
References
1.
McKusick VA: Heritable Disorders of Connective Tissue, ed. 4. St. Louis: Mosby, 1972.
Hunter GC, Malone JM, Moore WS, et al: Vascular manifestations in patients with Ehlers-Danlos syndrome . Arch Surg117:495-498, 1982.
4.
Leiner CV, Call TD, Fulkerson PK, et al: The spectrum of cardiac defects in the Ehlers-Danlos syndrome types I and III. Ann Intern Med92:171-178, 1980.
5.
Di Mario C, Zanchetta M., Maiolino P.: Coronary aneurysms in a case of Ehlers-Danlos syndrome. Jpn Heart J29:491-495, 1988.
6.
Lees MH, Menashe VD, Sunderland CO, et al: Ehlers-Danlos syndrome associated with multiple pulmonary artery stenosis and tortuous systemic arteries. J Pediatr75:1031-1036, 1969.
7.
Hollister DW : Heritable disorders of connective tissue: Ehlers-Danlos syndrome. Pediatr Clin North Am25:575-590, 1978.