Neuroradiological Characteristics in Patients with Mucopolysaccharidosis Type II: A Systematic Review

Introduction: Mucopolysaccharidosis (MPS) is an inherited metabolic disorder that is part of the lysosomal disorders; the main characteristic is the deficiency of lysosomal enzymes responsible for the degradation of glycosaminoglycans except for type II or Hunter syndrome, which is X-linked recessiv...

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Detalles Bibliográficos

Principais autores:	Yancarlos Ramos-Villegas, Loraine Quintana-Pájaro, Christian Meza-Valle, Mario Contreras-Arrieta, Huber Padilla-Zambrano, Tariq Janjua, Willem G Calderon-Miranda, Yelson A Picon-Jaimes, Julio Castillo-Blandino, Luis R Moscote-Salazar, Natalia Guevara-Moriones
Formato:	Artigo
Idioma:	Inglês
Publicado:	Jaypee Brothers Medical Publisher 2023-02-01
Series:	Journal of Medical Academics
Assuntos:	diagnostic imaging hunter syndrome mucopolysaccharidosis ii
Acceso en liña:	https://www.jmaacms.com/doi/JOMA/pdf/10.5005/jp-journals-11003-0118
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