amelogenesis imperfecta

Amelogenesis imperfecta is passed down through families as a dominant trait.

Researchers are looking for mutations in other genes that may also cause amelogenesis imperfecta.

Amelogenesis imperfecta is a condition in which enamel does not form properly or at all.

Answer: There are several conditions that can cause the lack of enamel, including a condition called amelogenesis imperfecta.

There are many different types of Amelogenesis imperfecta.

Another very rare side effect is amelogenesis imperfecta.

Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3).

Amelogenesis imperfecta can have different inheritance patterns depending on the gene that is altered.

The exact incidence of amelogenesis imperfecta is uncertain.

People afflicted with amelogenesis imperfecta have teeth with abnormal color: yellow, brown or grey.

Mutations in this gene cause autosomal-recessive hypomaturation amelogenesis imperfecta.

Amelogenesis imperfecta is a tooth development disorder in which the teeth are covered with thin, abnormally formed enamel.

Taurodontism is found in association with amelogenesis imperfecta, ectodermal dysplasia and tricho-dento-osseous syndrome.

Amelogenesis imperfecta presents with abnormal formation of the enamel or external layer of teeth.

Jalili syndrome is a genetic disorder characterized by the combination of cone-rod dystrophy of the retina and amelogenesis imperfecta.

Amelogenesis imperfecta is due to the malfunction of the proteins in the enamel: ameloblastin, enamelin, tuftelin and amelogenin.

Mutations in AMELX can cause amelogenesis imperfecta, a disorder of tooth enamel development.

Amelogenesis imperfecta may be inherited as an X-linked, autosomal dominant, or autosomal recessive genetic trait, depending on the type.

A mutation in FAM20A was reported to be associated with amelogenesis imperfecta, an inherited enamel defect, and gingival hyperplasia syndrome.

A mutation in this gene, which alters the normal splice pattern and results in premature termination of the encoded protein, has been associated with amelogenesis imperfecta.

Mutations in the related AMELX gene on the X chromosome cause X-linked amelogenesis imperfecta.

Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome (TDO) and amelogenesis imperfecta with taurodontism.

Mutations in the ENAM gene can give rise to autosomal dominant Amelogenesis imperfecta, indicating a role in Amelogenesis.

About 5% of amelogenesis imperfecta cases are caused by mutations in the AMELX gene and are inherited in an X-linked pattern.

Amelogenesis imperfecta is also inherited in an autosomal recessive pattern; this form of the disorder can result from mutations in the ENAM or MMP20 gene.