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Weismann-Netter-Stuhl syndrome in two siblings

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Abstract

Cases of Weismann-Netter-Stuhl syndrome involving the upper extremities and affecting siblings have rarely been reported. We present the radiological findings of Weismann-Netter-Stuhl syndrome in two siblings, with upper extremity involvement in one of them.

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References

  1. Robinow M, Johnson GF. The Weismann-Netter syndrome. Am J Med Genet 1988; 29:573–579.

    CAS  PubMed  Google Scholar 

  2. Tieder M, Manor H, Peshin J, Alon US. The Weismann-Netter-Stuhl syndrome: a rare pediatric skeletal dysplasia. Pediatr Radiol 1995; 25:37–40.

    CAS  PubMed  Google Scholar 

  3. Nores JM, Monsegu MH, de Masfrand V, Oberlin F, Denormandie P, Remy JM. Identification and classification of tibioperoneal diaphyseal toxopachyosteosis (Weismann-Netter-Stuhl syndrome): based on two new cases and a review of the literature. Eur J Radiol 1997; 24:71–76.

    Article  PubMed  Google Scholar 

  4. Weismann-Netter R, Rouaux Y. Tibioperoneal diaphysary toxopachyostosis (R. Weismann-Netter and L. Stuhl) in two sisters. Presse Med 1956; 64:790.

    CAS  PubMed  Google Scholar 

  5. Hary S, Houvenagel E, Vincent G. A case of Weismann-Netter and Stuhl toxopachyosteosis with new bone sites. Rev Rhum Mal Osteoartic 1992; 59:73–75.

    CAS  PubMed  Google Scholar 

  6. Leone G. A case of Weismann-Netter and Stuhl syndrome (“toxopachyostéose diaphysaire tibio-péroniere) Radiol Med (Torino) 1981; 67:463–466.

    Google Scholar 

  7. Coimbra AV, Filardi S, Fernandes SR, Marques-Neto JF, Samara AM. Weismann-Netter-Stuhl syndrome: first Brazilian case reports. Joint Bone Spine 2000; 67:539–543.

    Article  CAS  PubMed  Google Scholar 

  8. Krewer B. Dysmorphie jambière de Weismann-Netter. Chez deux vrais jumeaux. Presse Med 1961; 69:419–420.

    CAS  PubMed  Google Scholar 

  9. Weismann-Netter R, Stuhl L. Congenital osteopathy eventually familial defined especially by antero-posterior incurvation and thickening of both bones of the leg: diaphyseal tibio-peroneal toxopachyostosis. Presse Med. 1954; 62:1618–1622.

    Google Scholar 

  10. Amendola MA, Brower AC, Tisnado J. Weismann-Netter-Stuhl syndrome: toxopachyostéose diaphysaire tibio-péroniere. AJR Am J Roentgenol 1980; 135:1211–1215.

    CAS  PubMed  Google Scholar 

  11. Hiller HG. Weismann-Netter syndrome (Toxopachyostéose diaphysaire tibio-péroniere). Australas Radiol 1976; 20:174–175.

    CAS  PubMed  Google Scholar 

  12. Ravaille C, Ravaille Mauer ML. Un cas de toxopachyostéose diaphysaire tibio-péroniere unilatérale a manifestation néonatale. Arch Fr Pediatr 1966; 23:978–979.

    Google Scholar 

  13. Zakarian H, Ceccaldi M, Acquaviva PC, Sarrat P, Maestracci D. Maladie de Weismann-Netter et Stuhl. J Radiol 1989; 70:133–137.

    CAS  PubMed  Google Scholar 

  14. Azimi F, Bryan PJ. Weismann-Netter-Stuhl syndrome (toxopachyostéose diaphysaire tibio-péroniere). Br J Radiol 1974; 47:618–620.

    CAS  PubMed  Google Scholar 

  15. Babeau P, Tire J, Pras P, Serres J. Radioclinical aspects of tibio-tibial diaphyseal toxo-pachyosteosis. Weismann-Netter and Stuhl disease. Two new cases. J Radiol Electrol Med Nucl 1977; 58:605–608.

    CAS  PubMed  Google Scholar 

  16. Koller ME, Maurseth K, Haneberg B, Aarskog D. A familial syndrome of diaphyseal cortical thickening of the long bones, bowed legs, tendency to fracture and ichthyosis. Pediatr Radiol 1979; 8:3179–3182.

    Google Scholar 

  17. Heully F, Gaucher A, Gaucher P, Laurent J, Vautrin D. Une curieuse association: maladie de Weismann-Netter-Stuhl, maladie de Biermer, goitre congénital. Press Med 1967; 75:1577–1578.

    CAS  Google Scholar 

  18. Roca M, De Gregorgio MA, Toubiano P, Villa-Vieja JL. Le syndrome de Weismann-Netter-Stuhl. A propos de deux nouveaux cas. Ann Radiol [? YEAR]; 30:401–403.

  19. States LJ. Imaging of metabolic bone disease and marrow disorders in children. Radiol Clin North Am 2001; 39:749–772.

    CAS  PubMed  Google Scholar 

  20. Cheema I, Grissom LE, Harcke HT. Radiographic characteristics of lover-extremity bowing in children. Radiographics 2003; 23:871–880.

    PubMed  Google Scholar 

  21. Kozlowski K, Masel J. Mesomelic dysplasia with periosteal thickening, radio-humeral dislocation, osteoporosis and multiple fractures. Eur J Pediatr 1999; 158:308–311.

    Article  CAS  PubMed  Google Scholar 

  22. Hunter AG, Jarvis J. Osteofibrous dysplasia: two affected male sibs and an unrelated girl with bilateral involvement. Am J Med Genet. 2002; 112:79–85.

    Google Scholar 

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Correspondence to Ensar Yekeler.

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Yekeler, E., Ozdemir, C., Gokalp, S. et al. Weismann-Netter-Stuhl syndrome in two siblings. Skeletal Radiol 34, 176–179 (2005). https://doi.org/10.1007/s00256-004-0817-3

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  • DOI: https://doi.org/10.1007/s00256-004-0817-3

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