Background: There is an association between treatment options and growth in patients with mucopolysaccharidoses (MPS). The appropriate management of MPS is an essential factor for the growth of the patients. Objectives: This study aims to review systematically the available data on the growth status and related treatment factors in patients with MPS type I and MPS type II. Methods: A systematic literature search was performed in PubMed, Scopus, and the Web of Science using related keywords by March 2023. In this systematic review, the primary outcome was determining the growth status (mainly height z-score) of patients with MPSI and MPSII from reviewed studies and its association with different treatment options. The author’s name, year of ...
Introduction: Mucopolysaccharidosis type III (MPS III) is a rare disorder characterized by progressi...
The impact of hematopoietic stem cell transplantation (HSCT) on growth in patients diagnosed with mu...
Mucopolysaccharidosis-plus syndrome (MPS-PS) is a novel autosomal recessive disorder caused by a mut...
BackgroundThe skeletal phenotype of mucopolysaccharidosis VI (MPS VI) is characterized by short stat...
BACKGROUND: Mucopolysaccharidosis III (MPS III), known as Sanfilippo disease, is a lysosomal storage...
Children with mucopolysaccharidosis II (MPS II), also known as Hunter syndrome, an X-linked disorder...
Purpose. Mucopolysaccharidoses (MPS) are group of inherited lysosomal storage diseases caused by mut...
Abstract Background Mucopolysaccharidosis (MPS) type III (Sanfilippo syndrome) comprises a group of ...
Mucopolysaccharidosis (MPS) VI is an autosomal recessive lysosomal storage disorder arising from def...
Background and Methods: Growth failure is characteristic of untreated mucopolysaccharidosis type VI ...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is an X-linked, recessive, lysosomal storage...
Abstract Our objective was to assess how the diagnosis and treatment of mucopolysaccharidosis I (MPS...
Mucopolysaccharidosis IVA (MPS IVA) is a lysosomal storage disease caused by biallelic mutations in ...
In this study, we aimed to describe the natural history of mucopolysaccharidosis I
BackgroundMucopolysaccharidosis type I (MPS I) results in significant disease burden and early treat...
Introduction: Mucopolysaccharidosis type III (MPS III) is a rare disorder characterized by progressi...
The impact of hematopoietic stem cell transplantation (HSCT) on growth in patients diagnosed with mu...
Mucopolysaccharidosis-plus syndrome (MPS-PS) is a novel autosomal recessive disorder caused by a mut...
BackgroundThe skeletal phenotype of mucopolysaccharidosis VI (MPS VI) is characterized by short stat...
BACKGROUND: Mucopolysaccharidosis III (MPS III), known as Sanfilippo disease, is a lysosomal storage...
Children with mucopolysaccharidosis II (MPS II), also known as Hunter syndrome, an X-linked disorder...
Purpose. Mucopolysaccharidoses (MPS) are group of inherited lysosomal storage diseases caused by mut...
Abstract Background Mucopolysaccharidosis (MPS) type III (Sanfilippo syndrome) comprises a group of ...
Mucopolysaccharidosis (MPS) VI is an autosomal recessive lysosomal storage disorder arising from def...
Background and Methods: Growth failure is characteristic of untreated mucopolysaccharidosis type VI ...
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is an X-linked, recessive, lysosomal storage...
Abstract Our objective was to assess how the diagnosis and treatment of mucopolysaccharidosis I (MPS...
Mucopolysaccharidosis IVA (MPS IVA) is a lysosomal storage disease caused by biallelic mutations in ...
In this study, we aimed to describe the natural history of mucopolysaccharidosis I
BackgroundMucopolysaccharidosis type I (MPS I) results in significant disease burden and early treat...
Introduction: Mucopolysaccharidosis type III (MPS III) is a rare disorder characterized by progressi...
The impact of hematopoietic stem cell transplantation (HSCT) on growth in patients diagnosed with mu...
Mucopolysaccharidosis-plus syndrome (MPS-PS) is a novel autosomal recessive disorder caused by a mut...