Mucopolysaccharidosis (MPS) encompasses a group of rare lysosomal storage disorders that are associated with the accumulation of glycosaminoglycans in organs and tissues. Respiratory disorders occur in all MPS types. in these patients, the prevalence of obstructive sleep apnea syndrome (OSAS), which may confer additional morbidity, remains overlooked, and the results of the few existing studies are controversial. the present study aimed to characterize the prevalence of OSAS in patients with MPS types I, II, and VI in a reference center.Forty-five patients with MPS (I, n = 17; II, n = 16; and VI; n = 12) in the Centro de Referncia em Erros Inatos do Metabolismo, who underwent full-night polysomnography, were enrolled in a retrospective stud...
Sleep-disordered breathing (SDB) is a chronic condition characterized by repeated breathing pauses d...
Mucopolysaccharidosis type I (MPS I) is a rare lysosomal disorder caused by deficiency of alpha-L-id...
(1) Background: Mucopolysaccharidoses (MPS) are a heterogeneous group of lysosomal storage disorders...
Abstract The mucopolysaccharidoses (MPSs) are a group of inherited, metabolic disorders characterize...
To study the sleep characteristics, pulmonary function, and their relationships in an enzyme naive p...
There is a growing awareness, based on both research and clinical studies, that abnormal sleep and c...
Mucopolysaccharidosis type IVA (Morquio syndrome) is a multisystemic autosomal recessive transitive ...
Abstract: Obstructive sleep apnea (OSA) is a clinical picture characterized by repeated episodes of ...
Mucolipidosis II (Inclusion cell or I-cell disease) is an autosomal recessive lysosomal storage diso...
In mucopolysaccharidoses, upper airway obstruction has multiple causative factors and progressive re...
Objective: To determine the obstructive sleep apnea in patients with metabolic syndrome. Patients A...
Ekici, Arif B/0000-0001-6099-7066WOS: 000298342100016PubMed: 22171909Objective: Insulin resistance (...
Mucopolysaccharidosis type I (MPS I) is a rare lysosomal disorder caused by deficiency of alph-L-idu...
OBJECTIVE: Obstructive sleep apnea syndrome (OSAS) is an episodic disease that is characterized by i...
Childhood obstructive sleep apnea syndrome (OSAS) is characterized by anatomical and functional uppe...
Sleep-disordered breathing (SDB) is a chronic condition characterized by repeated breathing pauses d...
Mucopolysaccharidosis type I (MPS I) is a rare lysosomal disorder caused by deficiency of alpha-L-id...
(1) Background: Mucopolysaccharidoses (MPS) are a heterogeneous group of lysosomal storage disorders...
Abstract The mucopolysaccharidoses (MPSs) are a group of inherited, metabolic disorders characterize...
To study the sleep characteristics, pulmonary function, and their relationships in an enzyme naive p...
There is a growing awareness, based on both research and clinical studies, that abnormal sleep and c...
Mucopolysaccharidosis type IVA (Morquio syndrome) is a multisystemic autosomal recessive transitive ...
Abstract: Obstructive sleep apnea (OSA) is a clinical picture characterized by repeated episodes of ...
Mucolipidosis II (Inclusion cell or I-cell disease) is an autosomal recessive lysosomal storage diso...
In mucopolysaccharidoses, upper airway obstruction has multiple causative factors and progressive re...
Objective: To determine the obstructive sleep apnea in patients with metabolic syndrome. Patients A...
Ekici, Arif B/0000-0001-6099-7066WOS: 000298342100016PubMed: 22171909Objective: Insulin resistance (...
Mucopolysaccharidosis type I (MPS I) is a rare lysosomal disorder caused by deficiency of alph-L-idu...
OBJECTIVE: Obstructive sleep apnea syndrome (OSAS) is an episodic disease that is characterized by i...
Childhood obstructive sleep apnea syndrome (OSAS) is characterized by anatomical and functional uppe...
Sleep-disordered breathing (SDB) is a chronic condition characterized by repeated breathing pauses d...
Mucopolysaccharidosis type I (MPS I) is a rare lysosomal disorder caused by deficiency of alpha-L-id...
(1) Background: Mucopolysaccharidoses (MPS) are a heterogeneous group of lysosomal storage disorders...