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Orodental phenotype and genotype findings in all subtypes of hypophosphatasia.

Archive ouverte | Reibel, Amélie | CCSD

International audience. BACKGROUND: Hypophosphatasia (HP) is a rare inherited disorder characterized by a wide spectrum of defects in mineralized tissues and caused by deficiency in the tissue non-specific alkaline ...

A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

Archive ouverte | Prasad, Megana K. | CCSD

International audience. Background Orodental diseases include several clinically and genetically heterogeneous disorders that can present in isolation or as part of a genetic syndrome. Due to the vast number of gene...

Inequalities in treatment planning for children with intellectual disabilities: A questionnaire study of dentists in Europe

Archive ouverte | Camoin, Ariane | CCSD

International audience. Background: Children with intellectual disabilities experience major inequality in the field of oral health, including a higher number of extracted teeth. The literature explains this differe...

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