Amelogenesis Imperfecta, Type If; Ai1f

Description

Amelogenesis imperfecta type IF is characterized by hypoplastic enamel of the primary and secondary dentition. The teeth may appear rough and discolored, and the tooth enamel may be absent, pitted, or of varying thickness (Poulter et al. (2014)).

Clinical Features

Phenotypes and symptoms related to Amelogenesis Imperfecta, Type If; Ai1f

  • Hypoplasia of dental enamel
  • Amelogenesis imperfecta
  • Abnormality of dental color
  • Dental enamel pits

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.

Alternative names

Amelogenesis Imperfecta, Type If; Ai1f Is also known as amelogenesis imperfecta, hypoplastic type if, ai1f.

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 If; Ai1f Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Amelogenesis imperfecta type 1F.

By Centogene AG - the Rare Disease Company (Germany).

AMBN
Specificity
100 %
Genes
100 %
AMBN.

By Fulgent Genetics Fulgent Genetics (United States).

AMBN
Specificity
100 %
Genes
100 %

You can get up to -6 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like HYPERPROINSULINEMIA CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V; CMT2V WAISMAN SYNDROME; WSMN ACHONDROGENESIS, TYPE II; ACG2 BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER); PBD11A JOUBERT SYNDROME 20; JBTS20