Elucidation of the Sequence and the Genomic Organization of the Human Dentin Matrix Acidic Phosphoprotein 1 (DMP1) Gene: Exclusion of the Locus from a Causative Role in the Pathogenesis of Dentinogenesis Imperfecta Type II

Genomics ◽  
1997 ◽  
Vol 42 (1) ◽  
pp. 38-45 ◽  
Author(s):  
Karen L. Hirst ◽  
Darrin Simmons ◽  
Jian Feng ◽  
Helen Aplin ◽  
Michael J. Dixon ◽  
...  
Keyword(s):  
Genomic Organization ◽  
Causative Role ◽  
Type Ii ◽  
Dentinogenesis Imperfecta ◽  
Human Dentin ◽  
Dentin Matrix

Genomic Organization of the Human Osteopontin Gene: Exclusion of the Locus from a Causative Role in the Pathogenesis of Dentinogenesis Imperfecta Type II

Genomics ◽  
1995 ◽  
Vol 27 (1) ◽  
pp. 155-160 ◽  
Author(s):  
Andrew H. Crosby ◽  
Sara J. Edwards ◽  
Jeffrey C. Murray ◽  
Michael J. Dixon
Keyword(s):  
Genomic Organization ◽  
Causative Role ◽  
Type Ii ◽  
Dentinogenesis Imperfecta

The Non-collagenous Dentin Matrix Proteins are Involved in Dentinogenesis Imperfecta Type II (DGI-II)

2000 ◽  
Vol 79 (3) ◽  
pp. 835-839 ◽  
Author(s):  
S.R. Thotakura ◽  
T. Mah ◽  
R. Srinivasan ◽  
Y. Takagi ◽  
A. Veis ◽  
...  
Keyword(s):  
Matrix Proteins ◽  
Type Ii ◽  
Dentinogenesis Imperfecta ◽  
Dentin Matrix

Dentinogenesis Imperfecta type II: A case report

2014 ◽  
Vol 9 (2) ◽  
pp. 73-78
Author(s):  
P Moini ◽  
M Afsharianzadeh ◽  
E Abdoli Tafti
Keyword(s):  
Case Report ◽  
Type Ii ◽  
Dentinogenesis Imperfecta

Dentinogenesis Imperfecta Type II in Children: A Scoping Review

2019 ◽  
Vol 43 (3) ◽  
pp. 147-154 ◽  
Author(s):  
Arturo Garrocho-Rangel ◽  
Irma Dávila-Zapata ◽  
Ricardo Martínez-Rider ◽  
Socorro Ruiz-Rodríguez ◽  
Amaury Pozos-Guillén
Keyword(s):  
Scoping Review ◽  
Alveolar Bone ◽  
Genetic Disorders ◽  
Well Being ◽  
Pediatric Dentistry ◽  
Clinical Findings ◽  
Permanent Teeth ◽  
Type Ii ◽  
Dentinogenesis Imperfecta ◽  
Long Term Follow Up

Dentinogenesis Imperfecta type II (DI2), also known as hereditary opalescent dentin, is one of the most common genetic disorders affecting the structure of dentin, not related with osteogenesis imperfecta, which involves both primary and permanent dentitions. The purpose of this article is to perform a scoping review of the published peer-reviewed literature (1986–2017) on DI2 management in children and to outline the most relevant clinical findings extracted from this review. Forty four articles were included in the present scoping review. According to the extracted data, the following are the most important tasks to be performed in clinical pediatric dentistry: to re-establish the oral mastication, esthetics, and speech, and the development of vertical growth of alveolar bone and facial muscles; to reduce the tendency to develop caries, periapical lesions and pain; to preserve vitality, form, and size of the dentition; to avoid interfering with the eruption process of permanent teeth; to decrease the risk of tooth fractures and occlusion disturbances; to return the facial profile to a more normal appearance; and to prevent or treat possible temporomandibular joint problems. Therefore, Pediatric Dentists should bear in mind that early diagnosis and treatment, together a long-term follow-up of DI2 in children, continue to be the best approaches for achieving enhanced patient psychological well-being and, in consequence, their quality of life.

Genomic Organization of the Human Heparan Sulfate-N-Deacetylase/N-Sulfotransferase Gene: Exclusion from a Causative Role in the Pathogenesis of Treacher Collins Syndrome

Genomics ◽  
1996 ◽  
Vol 32 (3) ◽  
pp. 471-473 ◽  
Author(s):  
Amanda J. Gladwin ◽  
Jill Dixon ◽  
Stacie K. Loftus ◽  
John J. Wasmuth ◽  
Michael J. Dixon
Keyword(s):  
Heparan Sulfate ◽  
Genomic Organization ◽  
Treacher Collins Syndrome ◽  
Causative Role

Genomic Organization and Amplification of the Human Epidermal Type II Keratin Genes K1 and K5

2000 ◽  
Vol 274 (1) ◽  
pp. 149-152 ◽  
Author(s):  
Neil V. Whittock ◽  
Robin A.J. Eady ◽  
John A. McGrath
Keyword(s):  
Genomic Organization ◽  
Type Ii

DSPP mutation in dentinogenesis imperfecta Shields type II

10.1038/84765 ◽  
2001 ◽  
Vol 27 (2) ◽  
pp. 151-152 ◽  
Author(s):  
Xiaohai Zhang ◽  
Jun Zhao ◽  
Changfu Li ◽  
Shan Gao ◽  
Changchun Qiu ◽  
...  
Keyword(s):  
Type Ii ◽  
Dentinogenesis Imperfecta
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