Disorders

Amelogenesis Imperfecta, Type III

Synonym(s): ADHCAI, AI3, Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Dominant, Amelogenesis Imperfecta, Hypomineralization Type

OMIM

Gene	Locus	Protein
FAM83H	8q24.3	Protein FAM83H

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.