Literature DB >> 3771740

Familial variant of maxillonasal dysplasia?

E Gross-Kieselstein, Y Har-Even, P Navon, D Branski.   

Abstract

A rare syndrome comprising midfacial hypoplasia, lack of anterior nasal spine, and malocclusion is described. To the best of our knowledge, only sporadic cases with a similar cluster of defects have been reported, usually with the appellation of Binder syndrome. We describe an affected mother and daughter, thus suggesting a dominant mode of inheritance.

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Year:  1986        PMID: 3771740

Source DB:  PubMed          Journal:  J Craniofac Genet Dev Biol        ISSN: 0270-4145


  1 in total

1.  Binder's syndrome: Report of two cases.

Authors:  Hitesh Vij; Puneet Batra; Partha Sadhu; Ruchieka Vij
Journal:  Dent Res J (Isfahan)       Date:  2014-01
  1 in total

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