Mucopolysaccharidosis Type I: A Review of the Natural History and Molecular Pathology

Medicine and Dentistry

• Hurler Syndrome 100%
• Molecular Pathology 100%
• Symptom 60%
• Early Diagnosis 60%
• Disease 40%
• Glycosaminoglycan 40%
• Cells 20%
• Tissues 20%
• Development 20%
• Therapeutic Procedure 20%
• Infection 20%
• Cognitive Defect 20%
• Oxidative Stress 20%
• Pathogenesis 20%
• Phenotype 20%
• Patient 20%
• Organ 20%
• Homeostasis 20%
• Enzyme 20%
• Heparan Sulfate 20%
• Respiratory Disease 20%
• Heart Disease 20%
• Hearing 20%
• Absence 20%
• Autosomal Recessive Inheritance 20%
• Airway Obstruction 20%
• Dysplasia 20%
• Kyphosis 20%
• Lysosome 20%
• Levo Iduronidase 20%
• Nerve Fiber 20%
• Hernia 20%
• Infancy 20%
• Genetic Disorder 20%
• Collagen Fibril 20%
• Tissue Expansion 20%
• Rhinitis 20%
• Inflammation 20%
• Upper Respiratory Tract Obstruction 20%
• Dermatan Sulfate 20%
• Bone Malformation 20%

Biochemistry, Genetics and Molecular Biology

• Mucopolysaccharidosis 100%
• Life 40%
• Glycosaminoglycan 40%
• Comprehension 20%
• Development 20%
• Phenotype 20%
• Lysozyme 20%
• Animal Models 20%
• Homeostasis 20%
• Hearing 20%
• Bone 20%
• Collagen 20%
• Heparan Sulfate 20%
• Oxidative Stress 20%
• Dysplasia 20%
• Lysosome 20%
• Autosomal Recessive Inheritance 20%
• Infancy 20%
• Iduronidase 20%
• Dermatan Sulfate 20%

Neuroscience

• Hurler Syndrome 100%
• Glycosaminoglycan 40%
• Enzymes 20%
• Oxidative Stress 20%
• Respiratory Diseases 20%
• Cognitive Disorders 20%
• Phenotype 20%
• Collagen 20%
• Sensation of Hearing 20%
• Dysplasia 20%
• Levo Iduronidase 20%
• Lysosomes 20%
• Heparan Sulfate 20%
• Rhinitis 20%
• Dermatan Sulfate 20%