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The Prevalence of Behçet’s Syndrome and Its Neurological Complications in Hertfordshire, U.K.

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Book cover Adamantiades-Behçet’s Disease

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 528))

Conclusion

Behçet’s syndrome is uncommon in Hertfordshire and the prevalence is less than that in areas of the Silk Route but not as low as was previously thought. Since this county is typical of other UK counties, it is possible to surmise that the data reflect a national prevalence in the UK of some 1500 patients with the systemic manifestations of the disease and some 225 with neurological complications.

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References

  1. Yurdakul, S., Gunaydin, I., Tuzun, Y., et al., 1988, The prevalence of Behçet’s syndrome in a rural area in northern Turkey. J. Rheumatol. 15: 820–822.

    CAS  PubMed  Google Scholar 

  2. Yamamoto, S. I., Toykawa, H., Matsubara, J., et al., 1974, A nationwide survey of Behçet’s disease in Japan. An epidemiological survey. Jpn. J. Ophthalmol. 18: 282–290.

    Google Scholar 

  3. Zouboulis Ch.C., 1995, Habilitation thesis, Adamantiades-Behçet’s disease: Clinical and experimental findings in 53 patients from the Berlin area. Berlin.

    Google Scholar 

  4. Serdaroglu, P., Yazici, H., Özdemir, C., et al., 1989, Neurologic involvement in Behçet’s syndrome. A prospective study. Arch. Neurol. 46: 265–269.

    CAS  PubMed  Google Scholar 

  5. Benamour, S., Zeroual, B., Bennis, R., et al., 1990, Maladie de Behçet: 316 cas. Presse Med. 19: 1485–1489.

    CAS  PubMed  Google Scholar 

  6. Assaad-Khalil, S., Abou-Seif, M., Abou-Seif, S., et al., 1993, Neurologic involvement in Behçet’s disease: Clinical, genetic and computed tomographic study. In: Behçet’s disease (B. Wechsler, and P. Godeau, eds.), Excerpta Medica, Amsterdam, pp. 409–414.

    Google Scholar 

  7. Lakhanpal, S., Tani, K., Lie, J.T., et al., 1985, Pathologic features of Behçet’s syndrome: a review of Japanese autopsy registry data. Hum. Pathol. 16: 790–795.

    CAS  PubMed  Google Scholar 

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© 2004 Kluwer Academic Publishers

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Kidd, D. (2004). The Prevalence of Behçet’s Syndrome and Its Neurological Complications in Hertfordshire, U.K.. In: Zouboulis, C.C. (eds) Adamantiades-Behçet’s Disease. Advances in Experimental Medicine and Biology, vol 528. Springer, Boston, MA. https://doi.org/10.1007/0-306-48382-3_19

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  • DOI: https://doi.org/10.1007/0-306-48382-3_19

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-0-306-47757-7

  • Online ISBN: 978-0-306-48382-0

  • eBook Packages: Springer Book Archive

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