Intra-familial phenotype variant in hypoplastic amelogenesis imperfecta under a complex genetic component: a family report, whole-exome sequencing, and literature review

Abstract Amelogenesis imperfecta (AI) encompasses a group of conditions characterized by abnormalities in the development or function of tooth enamel. Clinical manifestations include different forms and degrees of enamel frailty, associated with sensitivity, tooth fractures, stains, abnormal tooth m...

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التفاصيل البيبلوغرافية

الحاوية / القاعدة:	Journal of Applied Oral Science
المؤلفون الرئيسيون:	Célia Regina Moreira LANZA, Artur Melo RODRIGUES, Iasmin Fonseca Tolentino MASCARENHAS, Talita Roberta Ferreira de SOUZA, Matheus Oliveira REIS, Felipe Morando AVELAR, Maria Raquel Santos CARVALHO, Vasco Ariston Carvalho de AZEVEDO, Debmalya BARH
التنسيق:	مقال
اللغة:	الإنجليزية
منشور في:	University of São Paulo 2025-09-01
الموضوعات:	Amelogenesis Imperfecta Enamel Tooth Gene ENAM
الوصول للمادة أونلاين:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572025000100302&lng=en&tlng=en