Clinical management of Hypoplasic Amelogenesis Imperfecta: a challenge for multidisciplinary team. A case report
Amelogenesis imperfecta (AI) refers to a group of rare genetic disorders that involve tooth development and are passed down through families. Hypoplasic AI phenotypes include the absence of enamel as a result of a defect in the secretory stage. This case report describes the diagnosis and treatment...
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| Main Authors: | , , |
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| Format: | Book |
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Universidad de Antioquia,
2021-02-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |