Peters-plus syndrome: oral health approach
The aim of this paper is to report a clinical case of a male patient with Peters-plus syndrome.
This syndrome is a rare, autosomal recessive congenital disorder. It is diagnosed by the
presence of ocular changes associated with delayed psychomotor development, cardiac
defects, and characteristic facial features, suc...
- Maíra Roberta Lima Viga, Emílio Carlos Sponchiado Júnior, Pollyanna Oliveira Medina, Ary de Oliveira Alves Filho, Simone Assayag Hanan
- 221-224
- Case report