Dentinogenesis imperfecta type II: an affected family saga.

Dentinogenesis imperfecta type II: an affected family saga. Research Abstract Details 

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Dentinogenesis imperfecta type II: an affected family saga. Abstract Text:

Mala Kamboj,Anil Chandra,Mala Kamboj,Anil Chandra,Mala Kamboj,Anil Chandra,

Dentinogenesis imperfecta (DI) type II or hereditary opalescent dentin is inherited in simple autosomal dominant mode with high penetrance and low mutation rate. It generally affects both the deciduous and permanent dentitions. DI type II corresponds to a localized form of mesodermal dysplasia, observed in histodifferentiation. Early diagnosis and treatment are therefore, fundamental, aiming at obtaining a favourable prognosis since late intervention makes treatment more complex. We present two cases of DI type II with the disease affecting three generations of a family in India, and briefly highlight the molecular basis of this disease. (J. Oral Sci. 49, 241-244, 2007).

Dentinogenesis imperfecta type II: an affected family saga. Publishing Authors By Initials

M Kamboj,A Chandra,M Kamboj,A Chandra,M Kamboj,A Chandra,

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Dentinogenesis imperfecta type II: an affected family saga. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: Journal of oral science

VOLUME: 49

Page Numbers: 241-4

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ISSN: 1343-4934

DAY: 11

MONTH: Sep

YEAR: 2007

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LANGUAGE: eng

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Grant and Affiliation Information for Dentinogenesis imperfecta type II: an affected family saga.

AFFILIATION: Department of Oral Pathology and Microbiology, U.P. King George's University of Dental Sciences.

Country: Japan

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MEDLINETA: J Oral Sci

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