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About 825 results

ALLMedicine™ Amelogenesis Imperfecta Center

Research & Reviews  411 results

A novel ENAM mutation causes hypoplastic amelogenesis imperfect.
https://doi.org/10.1111/odi.13877
Oral Diseases; Yu S, Zhang C et. al.

Apr 17th, 2021 - To identify the genetic cause of one Chinese family with hypoplastic amelogenesis imperfecta (AI) and explore the relationship between genotype and its phenotype. One Chinese family with generalized hypoplastic AI was recruited. One deciduous toot...

A novel homozygous SLC13A5 whole-gene deletion generated by Alu/Alu-mediated rearrangem...
https://doi.org/10.1002/ajmg.a.62192
American Journal of Medical Genetics. Part A; Duan R, Saadi NW et. al.

Apr 2nd, 2021 - Biallelic loss-of-function (LoF) of SLC13A5 (solute carrier family 13, member 5) induced deficiency in sodium/citrate transporter (NaCT) causes autosomal recessive developmental epileptic encephalopathy 25 with hypoplastic amelogenesis imperfecta ...

Management guidelines for amelogenesis imperfecta: a case report and review of the lite...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871387
Journal of Medical Case Reports; Roma M, Hegde P et. al.

Feb 9th, 2021 - Rehabilitation of the entire dentition with amelogenesis imperfecta (AI) tends to pose a great challenge to the clinician. Most of the cases of amelogenesis imperfecta are reported to be associated with skeletal and dental deformities which result...

A custom screw-retained implant-supported prosthesis for a patient with amelogenesis im...
https://doi.org/10.1016/j.prosdent.2020.12.021
The Journal of Prosthetic Dentistry; Bernal G, Salazar C et. al.

Feb 7th, 2021 - This clinical report with an 8-year follow-up describes the multidisciplinary management of a patient diagnosed with amelogenesis imperfecta. The rehabilitation included horizontal-guided bone regeneration, implant placement, use of a fixed interi...

Age-related dental phenotypes and tooth characteristics of FAM83H-associated hypocalcif...
https://doi.org/10.1111/odi.13780
Oral Diseases; Sriwattanapong K, Nitayavardhana I et. al.

Jan 24th, 2021 - Autosomal-dominant hypocalcified amelogenesis imperfecta (ADHCAI) shows phenotypic heterogeneity. Our aim was to characterise the ADHCAI phenotypes, tooth properties and genotypes. Three unrelated ADHCAI probands and seven additional affected memb...

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Clinicaltrials.gov  413 results

A novel ENAM mutation causes hypoplastic amelogenesis imperfect.
https://doi.org/10.1111/odi.13877
Oral Diseases; Yu S, Zhang C et. al.

Apr 17th, 2021 - To identify the genetic cause of one Chinese family with hypoplastic amelogenesis imperfecta (AI) and explore the relationship between genotype and its phenotype. One Chinese family with generalized hypoplastic AI was recruited. One deciduous toot...

A novel homozygous SLC13A5 whole-gene deletion generated by Alu/Alu-mediated rearrangem...
https://doi.org/10.1002/ajmg.a.62192
American Journal of Medical Genetics. Part A; Duan R, Saadi NW et. al.

Apr 2nd, 2021 - Biallelic loss-of-function (LoF) of SLC13A5 (solute carrier family 13, member 5) induced deficiency in sodium/citrate transporter (NaCT) causes autosomal recessive developmental epileptic encephalopathy 25 with hypoplastic amelogenesis imperfecta ...

Management guidelines for amelogenesis imperfecta: a case report and review of the lite...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871387
Journal of Medical Case Reports; Roma M, Hegde P et. al.

Feb 9th, 2021 - Rehabilitation of the entire dentition with amelogenesis imperfecta (AI) tends to pose a great challenge to the clinician. Most of the cases of amelogenesis imperfecta are reported to be associated with skeletal and dental deformities which result...

A custom screw-retained implant-supported prosthesis for a patient with amelogenesis im...
https://doi.org/10.1016/j.prosdent.2020.12.021
The Journal of Prosthetic Dentistry; Bernal G, Salazar C et. al.

Feb 7th, 2021 - This clinical report with an 8-year follow-up describes the multidisciplinary management of a patient diagnosed with amelogenesis imperfecta. The rehabilitation included horizontal-guided bone regeneration, implant placement, use of a fixed interi...

Age-related dental phenotypes and tooth characteristics of FAM83H-associated hypocalcif...
https://doi.org/10.1111/odi.13780
Oral Diseases; Sriwattanapong K, Nitayavardhana I et. al.

Jan 24th, 2021 - Autosomal-dominant hypocalcified amelogenesis imperfecta (ADHCAI) shows phenotypic heterogeneity. Our aim was to characterise the ADHCAI phenotypes, tooth properties and genotypes. Three unrelated ADHCAI probands and seven additional affected memb...

see more →

News  1 results

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

Sep 25th, 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...

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