What is Classical Ehlers-Danlos Syndrome? Classical EDS is a type of EDS, often caused by faulty collagen V. Classical EDS can be very variable even within the same family. It is a rare condition and therefore many health professionals will not have seen someone with this diagnosis. Classical EDS runs in families following a pattern called autosomal dominant inheritance, so in each pregnancy there is a 50% (1 in 2) chance of a child inheriting the altered copy of the gene and having Classical EDS. What are the main symptoms and signs of Classical EDS? Individuals with Classical EDS may have the following features: Joint hypermobility. Loose, unstable joints that can lead to dislocations and subluxations. Stretchy (hyperextensible) and fragile skin which can split easily. Smooth, velvety skin that bruises easily. Wounds can be slow to heal and leave distinctive widened scars. Fragile and extensible tissues can also result in hernias, prolapse and cervical insufficiency. Find out more on our website and please share this post to help raise awareness of Classical EDS during #EDSAwarenessMonth: bit.ly/1kRQDLt
Posted on: Sat, 10 May 2014 09:00:01 +0000