| Literature DB >> 1856834 |
I M Buntinx1, P J Willems, S E Spitaels, P J Van Reempst, A M De Paepe, J E Dumon.
Abstract
We describe a male neonate with severe arachnodactyly, hypermobility of the fingers, flexion contractures of elbows, wrists, hips, and knees, micrognathia, crumpled ears, rockerbottom feet, loose redundant skin, and ocular abnormalities. Severe cardiac valve insufficiency and aortic dilatation resulted in cardiac failure and death 20 hours after birth. This case represents the severe end of the clinical spectrum of Marfan syndrome. As similar patients have been reported, they may represent a separate mutation.Entities:
Mesh:
Year: 1991 PMID: 1856834 PMCID: PMC1016831 DOI: 10.1136/jmg.28.4.267
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318