Different Dental Manifestations in Sisters with the Same ALPL Gene Mutation: A Report of Two Cases

Hypophosphatasia (HPP) is an inherited disease caused by mutation of the alkaline phosphatase (ALPL) gene in an autosomal dominant or an autosomal recessive manner. The main symptoms of HPP are bone hypomineralization and early exfoliation of the primary teeth. Some of the mutations identified in au...

Descripción completa

Detalles Bibliográficos
Autores principales: Kadota, Tamami, Ochiai, Marin, Okawa, Rena, Nakano, Kazuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777029/
https://www.ncbi.nlm.nih.gov/pubmed/36553293
http://dx.doi.org/10.3390/children9121850

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777029/
https://www.ncbi.nlm.nih.gov/pubmed/36553293
http://dx.doi.org/10.3390/children9121850

Ejemplares similares