Amelogenesis Imperfecta, Type Iiib; Ai3b
Description
Hypomineralized amelogenesis imperfecta type IIIB is characterized by enamel that is reduced in mineral density and is thin, chipped, and absent in places (Smith et al., 2016).
Clinical Features
Phenotypes and symptoms related to Amelogenesis Imperfecta, Type Iiib; Ai3b
- Amelogenesis imperfecta
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Amelogenesis Imperfecta, Type Iiib; Ai3b Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 Amelotin deficiency.
By Centogene AG - the Rare Disease Company (Germany).
AMTN
Specificity
100 %
Genes
100 % |
 AMTN.
By Fulgent Genetics Fulgent Genetics (United States).
AMTN
Specificity
100 %
Genes
100 % |
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Learn moreSources and references
You can check the following sources for additional information.
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