Literature DB >> 3377000

The Weismann-Netter syndrome.

M Robinow1, G F Johnson.   

Abstract

The Weismann-Netter syndrome is a rare, heritable dysplasia of anterior bowing of tibiae and fibulae, often with lateral bowing of femora, short stature, and mild mental retardation. The condition is probably due to a primary metabolic abnormality of bone. The disease process is inactive in the adult. The pathogenesis is unknown. The patient reported here is the only child described in the Anglo-American literature.

Entities:  

Mesh:

Year:  1988        PMID: 3377000     DOI: 10.1002/ajmg.1320290315

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  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

北京卡尤迪生物科技股份有限公司 © 2022-2023.