Background Mucopolysaccharidosis type-III (MPS III) is an autosomal recessive lysosomal storage disorder. It causes progressive physical and cognitive decline and has been linked to increased incidences of behavioural problems. Methods Data on the behaviour and adaptive skills of 20 children with MPS III and 25 children with intellectual disability (ID) (17 included in analysis) were gathered via parental report questionnaire. The frequencies of different types of behaviour displayed by children with MPS III and children with ID were compared across two age categories. Results The total frequency of challenging behaviours displayed by children aged 2–9 years with MPS III and ID was not significantly different. Behaviours associated...
Objective: Mucopolysaccharidosis (MPS) IIIA (Sanfilippo syndrome type A) is a lysosomal storage diso...
There is a growing awareness, based on both research and clinical studies, that abnormal sleep and c...
In this study, we aimed to describe the natural history of mucopolysaccharidosis I
Mucopolysaccharidosis type IIIA (MPS IIIA, also known as Sanfilippo syndrome) is a rare genetic lyso...
Background: Mucopolysaccharidosis type IH (MPS-IH) [Hurlers Syndrome] is a developmental genetic dis...
The prevalence of autism spectrum disorder (ASD) in many genetic disorders is well documented but no...
BACKGROUND: The phenotypic spectrum of many rare disorders is much wider than previously considered....
Contains fulltext : 89262.pdf (publisher's version ) (Closed access)Mucopolysaccha...
Abstract Mucopolysaccharidoses (MPS) are a group of lysosomal multisystemic, chronic, and progressiv...
ObjectivesTo characterize the clinical course of mucopolysaccharidosis type IIIA (MPS IIIA), and ide...
Mucopolysaccharidosis type III (MPS III) is a rare genetic disorder caused by lysosomal storage of h...
Symptoms of autism spectrum disorder (ASD) are present in children with mucopolysaccharidosis type I...
Contains fulltext : 89261.pdf (publisher's version ) (Closed access)OBJECTIVE: Muc...
Mucopolysaccharidosis III (MPS III) is a rare inherited metabolic disease primarily affecting the ce...
Background: The phenotypic spectrum of many rare disorders is much wider than previously considered....
Objective: Mucopolysaccharidosis (MPS) IIIA (Sanfilippo syndrome type A) is a lysosomal storage diso...
There is a growing awareness, based on both research and clinical studies, that abnormal sleep and c...
In this study, we aimed to describe the natural history of mucopolysaccharidosis I
Mucopolysaccharidosis type IIIA (MPS IIIA, also known as Sanfilippo syndrome) is a rare genetic lyso...
Background: Mucopolysaccharidosis type IH (MPS-IH) [Hurlers Syndrome] is a developmental genetic dis...
The prevalence of autism spectrum disorder (ASD) in many genetic disorders is well documented but no...
BACKGROUND: The phenotypic spectrum of many rare disorders is much wider than previously considered....
Contains fulltext : 89262.pdf (publisher's version ) (Closed access)Mucopolysaccha...
Abstract Mucopolysaccharidoses (MPS) are a group of lysosomal multisystemic, chronic, and progressiv...
ObjectivesTo characterize the clinical course of mucopolysaccharidosis type IIIA (MPS IIIA), and ide...
Mucopolysaccharidosis type III (MPS III) is a rare genetic disorder caused by lysosomal storage of h...
Symptoms of autism spectrum disorder (ASD) are present in children with mucopolysaccharidosis type I...
Contains fulltext : 89261.pdf (publisher's version ) (Closed access)OBJECTIVE: Muc...
Mucopolysaccharidosis III (MPS III) is a rare inherited metabolic disease primarily affecting the ce...
Background: The phenotypic spectrum of many rare disorders is much wider than previously considered....
Objective: Mucopolysaccharidosis (MPS) IIIA (Sanfilippo syndrome type A) is a lysosomal storage diso...
There is a growing awareness, based on both research and clinical studies, that abnormal sleep and c...
In this study, we aimed to describe the natural history of mucopolysaccharidosis I