Ectopia lentis and aortic root dilatation in congenital contractural arachnodactyly.

Abstract

Congenital contractural arachnodactyly (CCA) was described by Beals and Hecht as an autosomal dominant disorder distinct from Marfan syndrome and comprising joint contractures, arachnodactyly, scoliosis, and a distinct "crumpled ear" deformity. While the disorder is similar to Marfan syndrome, it was split from it due to the distinct physical appearance of the patients and, more importantly, the lack of heart and eye findings. Since the original report, several CCA patients have been found to have mitral valve prolapse, structural cardiac anomalies, and occasionally aortic root dilatations similar to those seen in Marfan syndrome. We report on a patient with CCA with bilateral ectopia lentis and aortic root dilatation. Our review of the literature of CCA showed that serial echocardiography and careful eye examinations have not become a standard of medical practice in this condition. Partly this may be due to a lack of documented cases of CCA having severe ectopia lentis and cardiac complications. This patient underscores the need for periodic eye and echocardiographic evaluations of all CCA patients.

• Authors: E Bawle, M H Quigg
• Journal: American journal of medical genetics (Am J Med Genet) Vol. 42 Issue 1 Pg. 19-21 (Jan 01 1992) ISSN: 0148-7299 [Print] United States
• PMID: 1308360 (Publication Type: Case Reports, Journal Article)

Topics

• Aortic Aneurysm (complications, genetics)
• Child
• Ectopia Lentis (complications, genetics)
• Humans
• Male
• Marfan Syndrome (complications, genetics)
• Phenotype
• Syndrome
• Terminology as Topic