References
Bosque PJ, Vnencak-Jones CL, Johnson MD, Whitlock JA, McLean MJ (1992) A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt–Jakob disease. Neurology 42(10):1864–1870
Cervenakova L, Brown P, Piccardo P, Cummings JL, Nagle J, Vinters HV, Kaur P, Ghetti B, Chapman J, Gajdusek DC, Goldfarb LG (1996) 24-nucleotide deletion in the PRNP gene: analysis of associated phenotypes in transmissible subacute spongiform encephalopathies. In: Court L, Dodet B (eds) Elsevier, Paris, pp 433–444
Krasnianski A, Bartl M, Sanchez Juan PJ, Heinemann U, Meissner B, Varges D, Schulze-Sturm U, Kretzschmar HA, Schulz-Schaeffer WJ, Zerr I (2008) Fatal familial insomnia: Clinical features and early identification. Ann Neurol 63(5):658–661
Montagna P, Gambetti P, Cortelli P, Lugaresi E (2003) Familial and sporadic fatal insomnia. Lancet Neurol 2(3):167–176
Montagna P (2005) Fatal familial insomnia: a model disease in sleep physiopathology. Sleep Med Rev 9(5):339–353
Reder AT, Mednick AS, Brown P, Spire JP, Van Cauter E, Wollmann RL, Cervenàkovà L, Goldfarb LG, Garay A, Ovsiew F et al (1995) Clinical and genetic studies of fatal familial insomnia. Neurology 45(6):1068–1075
Spacey SD, Pastore M, McGillivray B, Fleming J, Gambetti P, Feldman H (2004) Fatal familial insomnia: the first account in a family of Chinese descent. Arch Neurol 61(1):122–125
Acknowledgment
Supported by the EU Network of Excellence “NeuroPrion” (FOOD-CT-2004-506579) and The Gino Galletti Foundation.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Baldin, E., Capellari, S., Provini, F. et al. A case of fatal familial insomnia in Africa. J Neurol 256, 1778–1779 (2009). https://doi.org/10.1007/s00415-009-5205-4
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00415-009-5205-4