Otodental Dysplasia

Known as: Chromosome 11q13 Deletion Syndrome, Otodental Syndrome 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1969-2016
012319692016

Papers overview

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2016
2016
BACKGROUND Orodental diseases include several clinically and genetically heterogeneous disorders that can present in isolation or… (More)
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2011
2011
We report on the first cases of FGF3 compound heterozygotes in two European families from non-consanguineous marriages, affected… (More)
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2005
2005
The purpose of this article is to describe the clinical features of otodental syndrome. A 9-year-old boy presented with dental… (More)
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1998
1998
A 12-year-old boy with characteristic findings of otodental syndrome is presented. Abnormalities of deciduous and permanent… (More)
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1998
1998
Three unusual dental anomalies are presented which should be of interest to the pediatric radiologist: otodental syndrome – an… (More)
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1996
1996
Otodental dysplasia, a form of ectodermal dysplasia, is characterized by abnormal dental crown morphology and sensorineural… (More)
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1994
1994
Fusion of either primary or permanent molars is rare. Fusion can be either partial or complete, depending on the developmental… (More)
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1987
1987
Double primary teeth were observed in 367 children and their relationship with the permanent successors was studied with the aid… (More)
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1981
1981
Peripheral auditory sensitivity is documented over a 5-year period on 4 cases with otodental dysplasia. Age of onset is noted for… (More)
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1976
1976
A family of Polish extraction was studied in which massive, globe-shaped posterior teeth were found in a father and two of his… (More)
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