Literature DB >> 471563

A familial syndrome of diaphyseal cortical thickening of the long bones, bowed legs, tendency to fracture and icthyosis.

M E Koller, K Maurseth, B Haneberg, D Aarskog.   

Abstract

The clinical and radiological features of a dominant bone disorder found in six members of the same family are described. The bone disorder was mainly characterized by endosteal cortical thickening of long tubular bones and bowing of the weight-bearing ones. The clinical symptoms were waddling gait, muscle weakness and leg pains, and there was a tendency to fractures. All affected individuals had icthyosis of slight or moderate degree.

Entities:  

Mesh:

Year:  1979        PMID: 471563     DOI: 10.1007/bf00973830

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  4 in total

1.  Hyperostosis corticalis generalisata congenita.

Authors:  H M Worth; D G Wollin
Journal:  J Can Assoc Radiol       Date:  1966-06

2.  Classification of osteogenesis imperfect.

Authors:  D O Sillence; D L Rimoin
Journal:  Lancet       Date:  1978-05-13       Impact factor: 79.321

3.  [Generalized hyperostosis corticalis (dominant transmission) (Worth's type)].

Authors:  P Maroteaux; G Fontaine; W Scharfman; J P Farriaux
Journal:  Arch Fr Pediatr       Date:  1971 Aug-Sep

4.  A new look at osteogenesis imperfecta. A clinical, radiological and biochemical study of forty-two patients.

Authors:  R J Bauze; R Smith; M J Francis
Journal:  J Bone Joint Surg Br       Date:  1975-02
  4 in total
  1 in total

1.  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
  1 in total

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