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| n |
A heterogeneous
group of hereditary
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disorders that
demonstrate developmental
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alterations in
the structure of enamel in the
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absence of a
systemic disorder
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| n |
Many subtypes
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| n |
Numerous patterns
of inheritance
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| n |
Wide variety of
clinical manifestations
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| n |
Frequency varies
between 1:718 and
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1:14,000
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| n |
Both dentitions
involved
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