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Myotonia Congenita (Thomsen's Disease) and Hereditary Psychosis

Published online by Cambridge University Press:  29 January 2018

John Johnson*
Affiliation:
Oldham and District General Hospital, Oldham, Lancs; University of Manchester

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
Copyright
Copyright © Royal College of Psychiatrists, 1967 

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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
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