The objective of this study was to report the clinical evaluation results and 3-dimensional (3-
D) dental and craniofacial characteristics observed in 2 male patients with …

Objective The aim was to assess craniofacial features through facial anthropometric and
lateral cephalometry measurements of individuals with mucopolysaccharidosis (MPS) and …

The correct diagnosis is fundamental for the appropriate treatment to be employed in a
particular pathology. The best treatment is not the one that solves only local problems …

Purpose This study described and compared the oral characteristics of Brazilian individuals
with mucopolysaccharidosis (MPS) and without MPS. Methods A cross-sectional study was …

Materials and Methods: The study included children affected with mucopolysaccharidosis
(n= 50) and healthy children (n= 50) in the control group between 3 and 15 years of age …

Abstract INTRODUÇÃO: A síndrome de Hunter é causada por mutações genéticas que
causam diminuição ou ausência de uma enzima específica, gerando acúmulo intracelular …

In resource-constrained settings, mucopolysaccharidosis (MPS) is a rare hereditary
metabolic illness that frequently remains undiagnosed. We present a scenario that illustrates …

Discussion The treatments used for childhood cancer, including chemotherapy, irradiation,
surgery, stem cell transplantation, and a combination of these modalities, have improved …

• Reilly en 1941 publicó su artículo" Los gránulos en los leucocitos del gargolismo",
relacionando las alteraciones que encontró en los linfocitos de pacientes con Enfermedad …

Objetivos: Descrever e comparar as características bucais de crianças/adolescentes com e
sem mucopolissacaridose (MPS). Métodos: Foi realizado um estudo transversal pareado …