×
About 430 results

ALLMedicine™ Amelogenesis Imperfecta Center

Research & Reviews  169 results

Management of Amelogenesis Imperfecta in Childhood: Two Case Reports.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8297319
International Journal of Environmental Research and Publi... Möhn M, Bulski JC et. al.

Jul 21st, 2021 - Amelogenesis imperfecta (AI) is defined as an interruption of enamel formation due to genetic inheritance. To prevent malfunction of the masticatory system and an unaesthetic appearance, various treatment options are described. While restoration w...

Interdisciplinary treatment of a patient with amelogenesis imperfecta: Case report with...
https://doi.org/10.1111/jerd.12804
Journal of Esthetic and Restorative Dentistry : Official ... Mathews DP, Knight DJ et. al.

Jul 13th, 2021 - This case will illustrate the interdisciplinary management of an adolescent female patient with amelogenesis imperfecta (AI). It will contrast this approach and compare it to the previous "multidisciplinary" treatment rendered before the patient w...

Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta.
https://doi.org/10.1177/00220345211015119
Journal of Dental Research; Kim YJ, Lee Y et. al.

May 27th, 2021 - Amelogenesis imperfecta (AI) is an innate disorder that affects the formation and mineralization of the tooth enamel. When diagnosed with AI, one's teeth can be hypoplastic (thin enamel), hypomature (normal enamel thickness but discolored and soft...

Two siblings with Heimler syndrome caused by PEX1 variants: follow-up of ophthalmologic...
https://doi.org/10.1080/13816810.2021.1923033
Ophthalmic Genetics; Herijgers D, Denayer E et. al.

May 7th, 2021 - Heimler syndrome (OMIM number #234580 and #616617) is a rare condition comprising sensorineural hearing loss (SNHL), nail abnormalities and amelogenesis imperfecta. In addition, patients with this syndrome can have retinal dystrophies. Heimler syn...

Kohlschütter-Tönz Syndrome With a Novel ROGD1 Variant in 3 Individuals: A Rare Clinical...
https://doi.org/10.1177/08830738211004736
Journal of Child Neurology; Akgün-Doğan Ö, Simsek-Kiper PO et. al.

Apr 20th, 2021 - Kohlschütter-Tönz syndrome (OMIM 226750) is a rare disorder with autosomal recessive inheritance among epileptic encephalopathy syndromes. To date, only 31 Kohlschütter-Tönz syndrome families have been reported in the literature. Early-onset epile...

see more →

Clinicaltrials.gov  2 results

Amelogenesis Imperfecta
https://clinicaltrials.gov/ct2/show/NCT01746121

Jul 11th, 2018 - Amelogenesis Imperfecta (AI) are a heterogeneous group of rare genetic diseases transmitted according to various mode of inheritance (X-linked, autosomal dominant, autosomal recessive) affecting the formation/mineralization of tooth enamel. These ...

Study of Factors of Genetic Susceptibility Associated to Severe Caries Phenotype
https://clinicaltrials.gov/ct2/show/NCT00541060

Dec 20th, 2010 - Although its prevalence has decreased dramatically in European countries, dental caries remains a burden for the society and especially for certain groups of the population. For example, 80% of the carious lesions are diagnosed in about 20% of the...

see more →

News  1 results

A Family With Malformed and Discolored Dentition
https://www.medscape.com/viewarticle/749907_2

Sep 26th, 2011 - Differential Diagnosis The presence of bulbous crowns and narrow roots, relatively normal density of any remaining enamel, and the obliteration of pulp chambers and root canals in the absence of marked attrition, are characteristic of dentinogenes...

see more →