Autor: |
Lyne, Alexandra, Parekh, Susan, Patel, Nikita, Lafferty, Fiona, Brown, Catriona, Rodd, Helen, Monteiro, Joana |
Zdroj: |
British Dental Journal; 20240101, Issue: Preprints p1-6, 6p |
Abstrakt: |
BackgroundAmelogenesis imperfecta (AI) is a genetic enamel defect that can affect both the primary and permanent dentition. It has a range of clinical phenotypes, and children and young people often present with challenging oral health needs. Patient-reported outcome measures (PROMs) can identify key patient concerns. |
Databáze: |
Supplemental Index |
Externí odkaz: |
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