Literature DB >> 6421022

[Diaphyseal dysplasia (Camurati-Engelmann)].

H Weickert, H Lehr, H S Braun.   

Abstract

Nine cases in three families with diaphyseal dysplasia are reported. In one family diaphyseal dysplasia and neurofibromatosis are combined. A lymphatic leucosis was found in one case. The possible autosomal recessive mode of inheritance in one family refer to heterogeneity in diaphyseal dysplasia.

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Year:  1983        PMID: 6421022     DOI: 10.1055/s-2008-1053306

Source DB:  PubMed          Journal:  Z Orthop Ihre Grenzgeb        ISSN: 0044-3220


  2 in total

1.  [Camurati-Engelmann disease (progressive diaphyseal dysplasia). Differential diagnostic problems].

Authors:  N Mastragelopulos; R Bähr; U Pfister
Journal:  Unfallchirurgie       Date:  1989-04

2.  Engelmann's disease with optic atrophy.

Authors:  J P Soni; B D Gupta; M Soni; V Mund; Rajesh Aneja
Journal:  Indian J Pediatr       Date:  2002-09       Impact factor: 1.967

  2 in total

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