Guest guest Posted January 12, 2004 Report Share Posted January 12, 2004 I see Jill has already posted some info. on this!! I also see that Laxity & I have found the same medical abstracts, as I posted the same abstract at the end of Dec.! A search on PubMed: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi , typing schievink wi (all lower case, & with a space between surname & initials), shows he has written many more papers on intracranial hypotension, with mention of both EDS, & Marfan syndrome. In particular, he seems to have found some that have this, also have some marfanoid skeletal features, & joint hypermobilty. A friend sent me another of his papers. This can be seen on Medscape: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi Fig. 1 shows a photo of a person with a connective tissue disorder, & joint hypermobilty, with their thumb touching their forearm! Sound familiar? In this paper, he lists symptoms of intracranial hypotension as being variable, including headache, neck stiffness, cranial nerve dysfunction, radicular arm pain, & symptoms of hindbrain herniation i.e. Chiari 1 Malformation. See: http://www.surgery.missouri.edu/ns/chiari/ Schievink, perhaps, has noted some with intracranial hypotension have Chiari 1, & a connective tissue disorder, but hasn't considered this association relevant. CSF leaks are associated with Chiari 1 Malformation. Chiari 1 Malformation has already been found to be associated with some connective tissue disorders such as achondroplasia, acro-osteolysis, Shprintzen-Goldberg syndrome, & in a few with osteogenesis imperfecta. Chiari 1 has also been found in some with Marfan syndrome, I have read from personal correspondence. However, of importance to us EDSers, it has been found there is an association between EDS, & Chiari. This is being studied, & written about now. At the Chiari Institute, NY, over 70 patients with Chiari 1 Malformation, have been found to also have EDS, in the last 2 years. Please note, only some of us with EDS, may also have Chiari 1 Malformation; I do not know the incidence, only that some with Chiari also have Classical/ Hypermobile/ Vascular EDS. Anyone interested, look at the wacma ( World Arnold Chiari Malformation Association) site: http://www.wacma.com/ ; consider joining the e-mail list : http://health.groups.yahoo.com/group/chiari/ , & see how often EDS is mentioned... on almost a daily basis. Also, if you join, you can search the archives for Ehlers-Danlos, or EDS. On a personal note, myself, eldest daughter, & son have HEDS. Our son's diagnosis has been revised to that of Marfanoid EDS, as he has some skeletal features of Marfan syndrome. Our son also has Chiari 1 Malformation. Our youngest daughter is now thought to have had a connective tissue disorder, such as EDS. She certainly had the cranial nerve dysfunction mentioned above. Due to the Chiari Malformation she's now thought to have had, her Xth cranial nerves were compressed, resulting in bilateral abductor vocal cord paralysis. Hoping this goes some way towards answering you queries, Lenore, Gail, North Yorkshire Quote Link to comment Share on other sites More sharing options...
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