Literature DB >> 10863398

Hypomaturation amelogenesis imperfecta: account of a family with an X-linked inheritance pattern.

E R Bundzman1, A Modesto.   

Abstract

Amelogenesis imperfecta (AI) is a heterogeneous genetic disorder which affects the dental enamel. It can have an autosomal dominant, autosomal recessive or X-linked pattern. The authors describe a case of a family with hypomaturation X-linked AI and discuss the clinical and histopathological aspects of this disorder.

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Year:  1999        PMID: 10863398

Source DB:  PubMed          Journal:  Braz Dent J        ISSN: 0103-6440


  1 in total

1.  Comprehensive rehabilitation of a case of Amelogenesis imperfecta.

Authors:  M Viswambaran; S M Londhe
Journal:  Med J Armed Forces India       Date:  2015-03-12
  1 in total

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