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Mucopolysaccharidosis, Type I
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Mucopolysaccharidosis, type I
Overview
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Skin conditions resulting from errors in metabolism
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type II
Gaucher disease
Fabry disease
Sialidosis
Phenylketonuria
Autosomal recessive disorders
(11)
Mucopolysa- ccharidosis type I Hurler syndrome
Mucopolysa- ccharidosis iii
Mucolipidoses
Mucopolysa- ccharidosis type VII
Multiple sulfatase deficiency
Multiple sulfatase deficiency
McArdle syndrome
Gangliosidosis
Isovaleric acidemia
Mucopolysa- ccharidosis iv
Gaucher disease
Phenylketonuria
more...
Genetic disorders
(19)
Myoclonic Epilepsy with Ragged Red Fibers
Multiple lentigines syndrome
Mucolipidosis III
Muscular dystrophy - Duchenne type
Spondyloepiphyseal dysplasia
Spondyloepiphyseal dysplasia
Genetic carrier
Mucopolysa- ccharidosis type I Hurler syndrome
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucolipidoses
Mucopolysa- ccharidosis, type II
Mucopolysa- ccharidosis type VII
Multiple sulfatase deficiency
Gaucher disease
Fabry disease
McArdle syndrome
Gangliosidosis
Isovaleric acidemia
Phenylketonuria
more...
Syndromes
Munchausens syndrome
Myelodysplastic syndromes
Mucopolysa- ccharidosis iii
Multiple lentigines syndrome
Mucopolysa- ccharidosis, type II
Mucopolysa- ccharidosis type VII
Hepatology
Hepatomegaly
Gaucher disease
Lysosomal storage diseases
(39)
Lysosomal storage disorders
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher disease
Glycogen storage disease type II
Glycoproteinosis
I-cell disease
Krabbe disease
Lipid storage disorder
Metachromatic leukodystrophy
Mucolipidoses
Mucolipidosis III
Mucolipidosis type IV
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis type I Hurler syndrome
Mucopolysa- ccharidosis type VII
Mucopolysa- ccharidosis, type II
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pycnodysostosis
Salla disease
Sandhoff disease
Schindler disease
Sialidosis
Tay-Sachs disease
Wolman disease
more...
Medical condition
(35)
Mucocutaneous lymph node disease
Myotonia atrophica
Myxomatous mitral valve
Muscle fasciculation
Infectious mononucleosis
Infectious mononucleosis
Myxoma
Alpha-l-iduronidase deficiency
Metatropic dwarfism
Inborn error of metabolism
Morvan disease
MPGN
Dysostosis
Curvature of the spine
Marinesco sjogren syndrome
Medulloblastoma
Meningococcal
Diabetes mellitus type 1
Meningioma
Myopathy
Malignant melanoma
Pectus carinatum
Mucopolysa- ccharidosis type I Hurler syndrome
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Munchausens syndrome
Mucolipidoses
Mucopolysa- ccharidosis, type II
Mucopolysa- ccharidosis type VII
Gaucher disease
Muscular dystrophy - Duchenne type
Fabry disease
Spondyloepiphyseal dysplasia
Sialidosis
Phenylketonuria
Myelodysplastic syndromes
more...
Hydrolases
(8)
Iduronate sulfatase
Beta galactosidase
Iduronidase
GALNS
N-acetylga- lactosamin- e-6-sulfatase
N-acetylga- lactosamine-6-sulfatase
Alpha-N-ac- etylglucosaminidase
Galsulfase
N-acetylgl- ucosamine-6-sulfatase
more...
Glycosaminoglycans
(9)
Dermatan
Heparan sulfate
Keratan sulfate
Mucopolysaccharides
Chondroitin sulfate
Chondroitin sulfate
Heparin
Heparinoid
Hyaluronan
Restylane
more...
Diseases and disorders
(12)
Maroteaux-Lamy syndrome
Joint stiffness
Growth failure
Mucous retention cyst
Megarectum
Megarectum
Macrocephaly
Mucopolysa- ccharidosis iv
Multiple sulfatase deficiency
Fabry disease
Dysostosis
Sialidosis
Gangliosidosis
more...
Symptoms
(13)
Movement dysfunctional
Motormental retardation
Muscle function loss
Uncoordinated movement
Coarse facial features
Coarse facial features
Short stature
Hearing impairment
Low nasal bridge
Mental retardation
Cloudy cornea
Muscle fasciculation
Joint stiffness
Growth failure
more...
Definition
MPS I S (Scheie syndrome)
MPS II, Hunter syndrome
MPS III (Sanfilippo syndrome)
MPS IV (Morquio syndrome)
Metabolism
See also
(20)
Monorchism
Myocardial contusion
Enzyme
Sulfatase
Galactosidase
Galactosidase
IVB
Metachromasia
Acetyl-CoA- :alpha-glucosaminide acetyltransferase
Midface trauma
Enzyme replacement therapy
Lysosomal
BioMarin
MPS II
Autosomal recessive
Acetylgalactosamine
Clouding
Electrocardiography
Genetic counseling
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