Simultaneous occurrence of duane retraction syndrome with marfan syndrome
- PMID: 22606474
- PMCID: PMC3350285
- DOI: 10.1155/2011/784259
Simultaneous occurrence of duane retraction syndrome with marfan syndrome
Abstract
Marfan syndrome (MFS) is an autosomal dominant disorder of connective tissue, while Duane retraction syndrome (DRS) is a congenital cranial dysinnervation disorder (CCDD) which can be transmitted as autosomal dominant disorder in 5-10% of patients. In this paper, we present an 8-year-old girl who presented with left eye DRS and bilateral subluxation of the lens associated with MFS in absence of familial involvement. To our knowledge this is the first case report of DRS with MFS. The occurrence of these syndromes together is very rare and appears to be coincidental.
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References
-
- Magenis RE, Maslen CL, Smith L, Allen L, Sakai LY. Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1. Genomics. 1991;11(2):346–351. - PubMed
-
- Pyeritz RE. Marfan syndrome. The New England Journal of Medicine. 1990;323(14):987–989. - PubMed
-
- De Paepe A, Devereux RB, Dietz HC, Hennekam RCM, Pyeritz RE. Revised diagnostic criteria for the Marfan syndrome. American Journal of Medical Genetics. 1996;62(4):417–426. - PubMed
-
- Rose PS, Levy HP, Ahm NU, et al. A comparison of the Berlin and Ghent nosologies and the influence of dural ectasia in the diagnosis of Marfan syndrome. Genetics in Medicine. 2000;2(5):278–282. - PubMed
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