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Twenty years-iowa muscle clinic: Reminiscences and prospects

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Abstract

The activities of the last twenty years of the Iowa clinic for neuromuscular diseases are briefly reviewed. Main emphasis in this paper is on management and guidance of the patient with Duchenne muscular dystrophy (DMD) by the families, the school and the public at large. Guidance and treatment given to our patients is briefly described. It is well known that chronic debilitating disease affects not only the patient but the whole family; management of DMD should therefore include the parents and siblings of the patient. Preventability of DMD is illustrated by the experiences in our clinic. The importance of early carrier detection and genetic counseling is stressed. Possible future developments in DMD research are briefly mentioned.

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References

  • Beckmann R, Robert JM, Zellweger H, Beubl L, Dellamonica C, Scheuerbrandt G (1980) Neonatal screening for muscular dystrophy. In: Screening for Inborn Errors of Metabolism, Springer, Berlin Heidelberg New York, pp 155–165

    Google Scholar 

  • Bickel H (1980) Commentary. In: Screening for Inborn Errors of Metabolism. Springer, Berlin Heidelberg New York, p 166

    Google Scholar 

  • Canki N, Dutrillaux B, Trivadar I (1979) Dystrophie musculaire de Duchenne chez une petite fille porteuse d'une translocation t(X;3)(p21:q13) de novo. Ann. Génét. 22:35–39

    Google Scholar 

  • Coulter DL (1980) The unfairness of life for children with handicaps. J.A.M.A. 244:1207–1208

    Google Scholar 

  • Duance VC, Stephens HR, Dunn M, Bailey AJ, Dubowitz V (1980) A role for collagen in the pathogenesis of muscular dystrophy? Nature 284:470–472

    Google Scholar 

  • Gardner-Medwin D (1980) Screening for Duchenne muscular dystrophy. Dev. Med. Child. Neurol. 22:246–247

    Google Scholar 

  • Greenstein RM, Reardon, MP, Chan TS, Middleton AB, Mulivor RA, Green AE, Coriell LL (1980) An (X;11) translocation in a girl with Duchenne muscular dystrophy. Cytogenet. Cell Genet. 27:268

    Google Scholar 

  • Huxley AF (1980) Future prospects. Br Med Bull 36:199–200

    Google Scholar 

  • Ionasescu V, Zellweger H, Conway TW (1971) Ribosomal protein synthesis in Duchenne muscular dystrophy. Arch. Biochem. Biophys. 144:51–58

    Google Scholar 

  • Ionasescu V, Zellweger H, Shirk P, Conway TW (1973) Identification of carriers of Duchenne muscular dystrophy. Neurol. 23:497–502

    Google Scholar 

  • Ionasescu V, Zellweger H, Ionasescu R, Lara-Braud, C (1977) Protein synthesis in human muscular dystrophy. In Proc. Fifth Internat. Conf. MDA (LP Rowland, Edit.), Excerpta Med. Internat. Congr. Ser. 404:362–375

  • Ionasescu V, Braga S, Rubenstein P, Kaeding L (1981) Muscle ribosome detachment factor. Acta Neurol. Scand. 64:108–121

    Google Scholar 

  • Jacobs PA, Hunt PA, Mayer M, Bart RD (1981) Duchenne muscular dystrophy (DMD) in a female with an X/autosomal translocation. Further evidence that the locus is at Cp21. Am. J. Hum. Genet. 33:513–518

    Google Scholar 

  • Lindenbaum RH, Clarke G, Patel C, Moncrieff, C, Hughes JT (1979) Muscular dystrophy in an X;1 translocation female suggests that Duchenne locus is on X chromosome short arm. J. Med. Genet. 16:389–392

    Google Scholar 

  • Lucy JA (1980) Is there a membrane defect in muscle and other cell? Brit. Med. Bull. 36:187–192

    Google Scholar 

  • Roses AD, Roses MJ, Miller SE, Hull KL, Appel SH (1976) Carrier detection in Duchenne muscular dystrophy. New Engl. J. Med 294:193–198

    Google Scholar 

  • Rowland LP (ed) (1977) Pathogenesis of the human muscular dystrophies. Excerpta Medica, Amsterdam

    Google Scholar 

  • Verellen CH, Markovic V, DeMeyer R, et al. (1978) Expression of an X-linked disease in a female due to non-random inactivation of the X chromosome. Am. J. Hum. Genet. 30: 97A (abstract).

    Google Scholar 

  • Zellweger H, Antonik A (1975) Newborn screening for Duchenne muscular dystrophy. Pediatrics 55:30–34

    Google Scholar 

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Herrn Prof. Dr. H.-R. Wiedemann, gewidmet zu seinem 65. Geburtstag

Curriculum vitae. Hans Zellweger, born in Lugano, Switzerland, graduated from the University of Zürich in 1934. After three years at the Kantonspital in Lucerne (Pathology, Microbiology) and two years with Dr. Albert Schweitzer in Lambarene he spent twelve years with Prof. G. Fanconi in the Kinderspital Zurich. He was general secretary of the International Congress of Pediatrics in Zurich, 1950. From 1951 to 1959 he was chairman of the Pediatrics Department of the American University in Beirut, Lebanon. Since 1959 he is Professor of Pediatrics at the University of Iowa, Iowa City, Iowa. He opened one of the first laboratories for cytogenetics in 1960. Thereafter he became director of the Genetic Clinic and founded a clinic for neuromuscular disease. In 1976 he organized with Jane Simpson the Regional Genetic Consultation Service for the whole State of Iowa, with fifteen genetic counseling clinics through the State of Iowa. He became Professor Emeritus in 1977, yet is still active in the genetic clinic. Dr. Victor Ionasescu is Director of the Clinic for Neuromuscular Diseases and Chief of the Laboratory for Muscle Research at the University of Iowa, Department of Pediatrics.

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Zellweger, H., Simpson, J. & Ionasescu, V. Twenty years-iowa muscle clinic: Reminiscences and prospects. Eur J Pediatr 138, 17–22 (1982). https://doi.org/10.1007/BF00442321

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