Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-31T14:24:49.786Z Has data issue: false hasContentIssue false
  • English
  • Français

Myotonia Congenita (Thomsen's Disease) and Hereditary Psychosis

Published online by Cambridge University Press:  29 January 2018

John Johnson
John Johnson*
Affiliation:
Oldham and District General Hospital, Oldham, Lancs; University of Manchester
Get access Rights & Permissions [Opens in a new window]

Extract

In 1876 the Danish physician, Julius Thomas Thomsen, described the disease entity of myotonia congenita, from which he himself and some members of his family suffered. This muscular disorder is now accepted as a clinical and genetic entity, distinct from other forms of myotonia, viz. dystrophia myotonica and paramyotonia (De Jong, 1955).

Type
Research Article
Information
The British Journal of Psychiatry , Volume 113 , Issue 502 , September 1967 , pp. 1025 - 1030
Copyright
Copyright © Royal College of Psychiatrists, 1967 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Adie, W. J., and Greenfield, J. G. (1923). “Dystrophia myotonica.” Brain, 46, 73.Google Scholar
Barwick, D. D., Osselton, J. W., and Walton, J. W. (1965). “Electroencephalographic studies in hereditary myopathy.” J. neurol. neurosurg. Psychiat., 28, 109.Google Scholar
Beard, A. W., and Slater, E. (1962). “Schizophrenialike psychoses of epilepsy.” Proc. roy. Soc. Med., 55, 311.CrossRefGoogle Scholar
Becker, P. E. (1966). Third Int. Congress of Genetics, Chicago, Sept. 5th–10th, 1966.Google Scholar
Bell, D. S. (1965). “Comparison of amphetamine psychoses and schizophrenia.” Brit. J. Psychiat., 111, 701.CrossRefGoogle ScholarPubMed
Bleuler, M. (1963). “Conceptions of schizophrenia within the last fifty years.” Proc. roy. Soc. Med., 56, 945.Google Scholar
De Jong, J. G. Y. (1955). Dystrophia Myotonica, Paramyotonia and Myotonia Congenita . Academic Dissertation, Utrecht. Van Garcum & Co.Google Scholar
Fish, F. J. (1962). Schizophrenia. Bristol: John Wright & Son.Google Scholar
Fish, F. J. (1964). “The cycloid psychoses.” Comprehensive Psychiatry, 5, 155.Google Scholar
Maas, O., and Paterson, A. S. (1939). “The identity of myotonia congenita, dystrophia myotonica and paramyotonia.” Brain, 62, 198.Google Scholar
Nissen, K. (1923). “Beiträge zur Kenntnis der Thomsen'schen Krankheit.” Ztschr. f. klin. Med., 97, 58.Google Scholar
Rossett, J. (1922). “A study of Thomsen's Disease.” Brain, 45, 1.Google Scholar
Sanders, J. (1935). “Eine Familie mit Myotonia Congenita.” Genetica, 17, 253.CrossRefGoogle Scholar
Slater, E. (1965). “Clinical aspects of genetic mental disorders.” In: Biochemical Aspects of Neurological Disorders. Ed. Cummings, J. M. and Kremer, M. Oxford: Blackwell.Google Scholar
Thomasen, E. (1948). Thomsen's Disease, Paramyotonia, Dystrophia Myotonica. Aarhus: Universitetsforlaget.Google Scholar
Thomsen, J. (1876). “Tonische Krämpfe in willkürlich beweglichen Muskeln in Folge von ererbter psychischer Disposition.” Arch. f. Psychiat., 76, 702.CrossRefGoogle Scholar
Vanier, J. M. (1960). “Dystrophia mytonica in childhood.” Brit. med. J., ii, 1284.Google Scholar
Submit a response

eLetters

No eLetters have been published for this article.