Literature DB >> 1579849

[A case of Weismann-Netter and Stuhl toxopachyosteosis with new bone sites].

S Hary1, E Houvenagel, G Vincent.   

Abstract

A case of Weismann-Netter-Stuhl toxopachyosteosis in a 63-year-old man is reported. Bone deformities had been present since the age of 18 months. Tibio-fibular dysmorphism was severe. Radiological evaluation revealed other lesions encountered more rarely: bilateral femoral incurvature and exostoses, bilateral coxa vara, radio-ulnar incurvature and flattening of the last ribs. Two other previously undescribed lesions were seen in this patient; bradymetacarpism of the last four rays of the left hand and dysmorphic lengthening of the left patella. This case illustrates the widespread nature and unusual extent of bone lesions in the context of toxopachyosteosis.

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Year:  1992        PMID: 1579849

Source DB:  PubMed          Journal:  Rev Rhum Mal Osteoartic        ISSN: 0035-2659


  3 in total

1.  The Weismann-Netter, Stuhl syndrome: a rare pediatric skeletal dysplasia.

Authors:  M Tieder; H Manor; J Peshin; U S Alon
Journal:  Pediatr Radiol       Date:  1995

2.  Weismann-Netter-Stuhl syndrome in two siblings.

Authors:  Ensar Yekeler; Candan Ozdemir; Selman Gokalp; Abdurrahman Yildirim; Firdevs Bas; Hulya Gunoz; Gulden Acunas
Journal:  Skeletal Radiol       Date:  2004-10-22       Impact factor: 2.199

3.  Weismann-Netter-Stuhl syndrome: a family report.

Authors:  Hayrullah Alp; Mehmet Emre Atabek; Özgür Pirgon
Journal:  J Clin Res Pediatr Endocrinol       Date:  2009-05-06
  3 in total

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