TY  - JOUR
AU  - Quijada-Fraile, Pilar
AU  - Arranz Canales, Elena
AU  - Martín-Hernández, Elena
AU  - Ballesta-Martínez, María Juliana
AU  - Guillén-Navarro, Encarna
AU  - Pintos-Morell, Guillem
AU  - Moltó-Abad, Marc
AU  - Moreno-Martínez, David
AU  - García Morillo, Salvador
AU  - Blasco-Alonso, Javier
AU  - Couce, María Luz
AU  - Gil Sánchez, Ricardo
AU  - Cortès-Saladelafont, Elisenda
AU  - López Rodríguez, Mónica A
AU  - García-Silva, María Teresa
AU  - Morales Conejo, Montserrat
PY  - 2021
DO  - 10.1186/s13023-021-02074-y
UR  - https://hdl.handle.net/10668/24505
T2  - Orphanet journal of rare diseases
AB  - Mucopolysaccharidosis (MPS) IVA or Morquio A syndrome is a progressive and disabling disease characterized by a deficiency of the enzyme N-acetylgalactosamine-6-sulphate sulphatase. Its clinical presentation is very heterogeneous and poorly understood...
LA  - en
KW  - Elosulfase alfa
KW  - Health-related quality of life
KW  - Mobility
KW  - Morquio A syndrome
KW  - Mucopolysaccharidosis IVA
KW  - Adult
KW  - Enzyme Replacement Therapy
KW  - Hip Dislocation
KW  - Humans
KW  - Mucopolysaccharidosis IV
KW  - Quality of Life
KW  - Self Care
KW  - Young Adult
TI  - Clinical features and health-related quality of life in adult patients with mucopolysaccharidosis IVA: the Spanish experience.
TY  - research article
VL  - 16
ER  -