Skip to main content
Log in

Ullrich's congenital atonic sclerotic muscular dystrophy

A case report

  • Original Investigations
  • Published:
Journal of Neurology Aims and scope Submit manuscript

Summary

A 5-year old girl with Ullrich's atonic-sclerotic muscular dystrophy is reported and 16 previously reported cases are reviewed. The clinical features, in particular proximal contractures, distal hyperextensibility, mild dysmorphism and hyperhidrosis, allow recognition of this subtype of congenital muscular dystrophy, which has no specific pathological characteristics. There is evidence in favour of an autosomal recessive mode of inheritance.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Donner M, Rapola J, Somer H (1975) Congenital muscular dystrophy: a clinico-pathological and follow-up study of 15 patients. Neuropädiatrie 6:239–258

    Google Scholar 

  2. Dubowitz V (1980) The floppy infant, 2nd edn. Spastics International Medical Publications, London

    Google Scholar 

  3. Fukuyama Y, Kawazura M, Haruna H (1960) A peculiar form of congenital progressive muscular dystrophy. Report of 15 cases. Pediatria (Univ Tokyo) 4:5–8

    Google Scholar 

  4. Gött H, Josten EA (1954) Beitrag zur kongenitalen atonischskerotischen Muskeldystrophie (Typ Ullrich). Monatsschr Kinderheilkd 75:105–116

    Google Scholar 

  5. Jones R, Khan R, Hughes S, Dubowitz V (1979) Congenital muscular dystrophy: the importance of early diagnosis and orthopaedic management in the long-term prognosis. J Bone Joint Surg 61:13–17

    Google Scholar 

  6. Nihei K, Kamoshita S, Atsumi T (1979) A case of Ullrich disease (Kongenitale, atonisch-sklerotische Muskeldystrophie). Brain Dev 1:61–67

    Google Scholar 

  7. Schneider H (1957) Die atonisch-sklerotische Muskeldystrophie (Ullrich) im Rahmen mesodermaler Dysplasien. Z Orthop 88:397–404

    Google Scholar 

  8. Segawa M (1970) Clinical studies of congenital muscular dystrophy. Arthrogrypotic type of congenital muscular dystrophy with mental retardation and facial muscle involvement. Brain Dev 2:439–451

    Google Scholar 

  9. Segawa M, Fukuyama Y, Itoh K, Vono M (1970) Congenital muscular dystrophy with progressive development of joint contracture, mental retardation and facial involvement. I. Clinical studies. Brain Dev 2:67

    Google Scholar 

  10. Stoeber E (1939) Über atonisch-sklerotische Muskeldystrophie (Typ Ullrich). Z Kinderheilkd 60:279–284

    Google Scholar 

  11. Ullrich O (1930) Kongenitale, atonisch-sklerotische Muskeldystrophie. Ein weiteres Typus der heredodegenerativen Erkrankungen des neuromuskulären Systems. Z Gesamte Neurol Psychiatr 126:171

    Google Scholar 

  12. Vassella F, Mumenthaler M, Rossi E, Moser H, Weissman U (1967) Die kongenitale Muskeldystrophie. Dtsch Z Nervenheilkd 190:349–374

    Google Scholar 

  13. Walton JN, Gardner-Medwin D (1974) Progressive muscular dystrophy and the myotonic disorders. In: Walton JN (ed) Disorders of voluntary muscle, 3rd edn. Churchill Livingstone, Edinburgh

    Google Scholar 

  14. Zellweger H, Afifi A, McCormick WF, Mergner W (1967) Benign congenital muscular dystrophy: a special form of congenital hypotonia. Clin Pediatr 6:655–663

    Google Scholar 

  15. Zellweger H, Afifi A, McCormick WF, Mergner W (1967) Severe congenital muscular dystrophy. Am J Dis Child 114:591–612

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

De Paillette, L., Aicardi, J. & Goutières, F. Ullrich's congenital atonic sclerotic muscular dystrophy. J Neurol 236, 108–110 (1989). https://doi.org/10.1007/BF00314406

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00314406

Key words

Navigation