Cadena Arteaga, Jorge AlejandroLasso Andrade, Fabricio AndresAchicanoy Puchana, Denny MarcelaAchicanoy Puchana, Diana FernandaCaicedo Morillo, Gina NataliaMedina-Bravo, Paola AndreaJuez Neira, William FernandoVanegas Bastidas, Cristian RicardoMontoya Ríos, Diana CarolinaVasquez Correa, Karen JuliethSuárez Cuéllar, Laura CatalinaOsorio Segura, Lady Johana2022-02-092022-02-092022-021930-0433https://hdl.handle.net/20.500.12495/6777Mucopolysaccharidosis type IV or Morquio Syndrome, is a lysosomal deposit disease, of autosomal recessive inheritance with a similar incidence in men and women. The clinical picture is of variable expressiveness, its phenotype is characterized by skeletal dysplasia that includes neck and short trunk, short stature, keel thorax, kyphosis, scoliosis, genus valgus, flat foot, coxa valga, gait disorders, instability of the cervical spine and wedge or ovoid vertebrae. The treatment is symptomatic, with enzyme replacement. We present a series of 5 cases, the product of 2 couples, with a confirmed diagnosis of Mucopolysaccharidosis type IV, and different clinical presentation.application/pdfengAttribution-NonCommercial-NoDerivatives 4.0 InternacionalSíndrome de morquioMucopolisacaridosisBaja estaturaGlicosaminoglicanosArtículo de revistaMorquio syndromeMucopolysaccharidosisShort statureGlycosaminoglycanshttps://doi.org/10.1016/j.radcr.2021.11.012instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquerepourl:https://repositorio.unbosque.edu.coAcceso abiertohttps://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessAcceso abierto