Skip to main content
SpringerLink
Log in

Zur Genetik der Epilepsien

  • Chapter
Der Anfallskranke in der ärztlichen Sprechstunde

Part of the book series: Kliniktaschenbücher ((KTB))

  • 17 Accesses

Zusammenfassung

Die Genetik der Epilepsien kann nur dann verstanden werden, wenn die Formalgenetik des multifaktoriellen Systems bekannt ist. Dieses Modell soll daher eingangs kurz dargestellt werden.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Log in via an institution
Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 54.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 69.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literatur

  1. Anderson VE (1982) Family studies of epilepsy. In: Anderson VE, Hauser WA, Penry JK, Sing CF (eds) Genetic basis of the epilepsies. Raven Press, New York, p 103–112

    Google Scholar 

  2. Bickel H, Cleve H (1967) Metabolische Schwachsinnsformen. In: Becker PE (Hrsg) Handbuch der Humangenetik Vol V/2. Thieme, Stuttgart S 206–339

    Google Scholar 

  3. Crowe FW, Schull WJ, Neel JV (1956) A clinical, pathological and genetic study of multiple neurofibromatosis. Charles C Thomas, Springfield, 111.

    Google Scholar 

  4. Doose H (1981) Special problems of genetic counseling. In: Gross-Selbeck G, Doose H (eds) Epilepsy-problems of marriage, pregnancy, genetic counseling. Thieme, Stuttgart New York, p 98–103

    Google Scholar 

  5. Fuhrmann W (1974) Die formale Genetik des Menschen. In: Vogel F (Hrsg) Handbuch der allgemeinen Pathologie. Vol. IX, Erbgefüge. Springer, Berlin Heidelberg New York, S147–259

    Google Scholar 

  6. Galton F (1865) Hereditary talent and character. Macmillan’s Magazine 12:157

    Google Scholar 

  7. Gomez MR (1979) Neurologic and psychiatric symptoms. In: Gomez MR (ed) Tuberous sclerosis. Raven Press, New York, p 85–93

    Google Scholar 

  8. Hayden MR (1981) Huntington’s Chorea. Springer, Berlin Heidelberg New York

    Book  Google Scholar 

  9. Holzinger KJ (1929) The relative effect of nature influences on twin differences. J Educat Psycol 20: 241–248

    Article  Google Scholar 

  10. Janz D, Beck-Mannagetta G (1982) Epilepsy and neonatal seizures in the offspring of parents with epilepsy. In: Anderson VE, Hauser WA, Penry JK, Sing CF (eds) Genetic Basis of the Epilepsies. Raven Press, New York, p 135–143

    Google Scholar 

  11. Koch G (1955) Krampfbereitschaft. Analecta Genetica, Rom

    Google Scholar 

  12. Koch G (1967) Epilepsien. In: Becker PE (Hrsg) Handbuch der Humangenetik, Vol V/2 Psychiatrische Krankheiten. Thieme, Stuttgart, S1–83

    Google Scholar 

  13. Lenz W (1979) Medizinische Genetik. 4. Aufl. Thieme, Stuttgart

    Google Scholar 

  14. McKusick VA (1978) Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes. The Johns Hopkins Univ Press, Baltimore London

    Google Scholar 

  15. Mendel G (1866) Versuche über Pflanzenhybriden. Verhandlungen des Naturforschenden Vereins (Brunn) 4:3–47

    Google Scholar 

  16. Nielsen J, Pedersen E (1969) Electro-encephalographic findings in patients with Klinefelter’s syndrome and the XYY syndrome. Acta Neurolog Scand 45:87–94

    Article  CAS  Google Scholar 

  17. Pfeiffer RA, Palm D, Jochmus J (1967) Das Erscheinungsbild der Trisomie des X-Chromosoms bei Jugendlichen (Triple-X-Syndrom). Mschr Kinderheilk 115:9–18

    PubMed  CAS  Google Scholar 

  18. Smeraldi E, Scorza-Smeraldi R, Cazzullo CL, Guareschi-Cazzullo, Canger R (1976) A genetic approach to the Lennox-Gastaut syndrome by the „Major Histocompatibility Complex“ (MHC). In: Janz D (ed) Epileptology. Thieme, Stuttgart, p 33

    Google Scholar 

  19. Vogel F, Helmhold W (1972) Blutgruppen — Populationsgenetik und Statistik. In: Becker PE Handbuch der Humangenetik, Vol 1/4 Blutgruppen, Thieme, Stuttgart, S129–557

    Google Scholar 

  20. Vogel F, Propping P (1981) Ist unser Schicksal mitgeboren? Severin & Siedler, Berlin

    Google Scholar 

Download references

Authors
  1. H.-D. Rott
    View author publications

    You can also search for this author in PubMed Google Scholar

Editor information

Editors and Affiliations

  1. Nervenkrankenhaus Bayreuth, Cottenbacher Straße 23, D-8580, Bayreuth, Deutschland

    Bernhard Kügelgen  & August Hillemacher  & 

Rights and permissions

Reprints and permissions

Copyright information

© 1984 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Rott, HD. (1984). Zur Genetik der Epilepsien. In: Kügelgen, B., Hillemacher, A. (eds) Der Anfallskranke in der ärztlichen Sprechstunde. Kliniktaschenbücher. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-95446-7_3

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-95446-7_3

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-12950-9

  • Online ISBN: 978-3-642-95446-7

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics

Search

Navigation