Disorders


 

Amelogenesis Imperfecta, Type IV


Synonym(s): AI4, AIHHT, Amelogenesis Imperfecta, Hypomaturation-Hypoplastic Type, with Taurodontism

 

OMIM

GeneLocusProtein
DLX317q21.33Homeobox protein DLX-3

Laboratory Test Method Prenatal Carrier *
ATG-GenMed - Berlin, Germany• Sequence analysis of the entire coding region
  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA• Deletion/duplication analysis
  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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