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Otodental Dysplasia

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

Papers overview

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2016
2016
Background Orodental diseases include several clinically and genetically heterogeneous disorders that can present in isolation or… Expand
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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… Expand
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Review
2006
Review
2006
The otodental syndrome also named otodental dysplasia, is characterised by a striking dental phenotype known as globodontia… Expand
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Review
2001
Review
2001
A 5-year-old boy presented with otodental syndrome. His maxillary and mandibular incisors were within normal limits. The premolar… Expand
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1998
1998
todental syndrome, also named oto-dentodysplasia, ~ otodental 2-4 dysplasia,and globodontia,5’ 6 has been reported as atype of… Expand
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1998
1998
Abstract Three unusual dental anomalies are presented which should be of interest to the pediatric radiologist: otodental… Expand
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1998
1998
A 12-year-old boy with characteristic findings of otodental syndrome is presented. Abnormalities of deciduous and permanent… Expand
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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… Expand
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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… Expand
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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… Expand
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