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Chapter 12 - Geneticcounseling for FTD

from Section 3 - Approach to the diagnosis of FTD

Published online by Cambridge University Press:  05 May 2016

By
Jill S. Goldman  and
Elisabeth McCarty Wood
Edited by
Bradford C. Dickerson
Bradford C. Dickerson
Affiliation:
Department of Neurology, Massachusetts General Hospital
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Hodges' Frontotemporal Dementia , pp. 153 - 164
Publisher: Cambridge University Press
Print publication year: 2016

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References

National Society of Genetic Counselors’ Definition Task Force, Resta, R, Biesecker, BB, Bennett, RL, et al. A new definition of Genetic Counseling: National Society of Genetic Counselors’ Task Force report. J Genet Couns 2006;15(2):77–83.CrossRefGoogle ScholarPubMed
Goldman, JS, Farmer, JM, Van Deerlin, VM, et al. Frontotemporal dementia: genetics and genetic counseling dilemmas. Neurologist 2004;10(5):227–34.CrossRefGoogle ScholarPubMed
McCarty-Wood, E. The role of genetics: a piece in the FTD puzzle. In Radin, G, Radin, L, eds. What If It's Not Alzheimer's? A Caregivers Guide to Dementia, 3rd edn. Amherst, NY: Prometheus Books. 2014; 62–79.Google Scholar
Goldman, JS, Farmer, JM, Wood, EM, et al. Comparison of family histories in FTLD subtypes and related tauopathies.Neurology 2005;65(11):1817–19.Google Scholar
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Wood, EM, Falcone, D, Suh, E, et al. Development and validation of pedigree classification criteria for frontotemporal lobar degeneration. JAMA Neurol 2013;70(11):1411–17.CrossRefGoogle ScholarPubMed
Hahn, SE. Primer on genetic counselling. Continuum (Minneap Minn.) 2011;17(2 Neurogenetics):268–79.Google Scholar
International Huntington Association and World Federation of Neurology. International Huntington Association and the World Federation of Neurology Research Group on Huntington's Chorea. Guidelines for the molecular genetics predictive test in Huntington's disease. J Med Genet 1994;31(7):555–9.Google Scholar
Le Ber, I, Camuzat, A, Guillot-Noel, L, et al. C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing. J Alzheimers Dis 2013;34(2):485–99.Google Scholar
Van Langenhove, T, van der Zee, J, Gijselinck, I, et al. Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort. JAMA Neurol 2013;70(3):365–73.Google Scholar
Goldman, JS, Rademakers, R, Huey, ED, et al. An algorithm for genetic testing of frontotemporal lobar degeneration. Neurology 2011;76(5):475–8.CrossRefGoogle ScholarPubMed

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