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Mps I
Mucopolysaccharidosis
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Related in the Kosmos
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Lysosomal storage diseases
(40)
Lysosomal storage disorder
MPS II
Mucolipidoses
Mucopolysa- ccharidosis ii
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis vii
Mucopolysa- ccharidosis, type I
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
I-cell disease
Krabbe disease
Lipid storage disorder
Metachromatic leukodystrophy
Mucolipidosis type IV
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Schindler disease
Sialidosis
Tay-Sachs disease
Wolman disease
more...
Autosomal recessive disorders
McArdle syndrome
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Mucopolysa- ccharidosis vii
Mucolipidoses
MPS II
Genetic disorders
(11)
Myoclonic Epilepsy with Ragged Red Fibers
Multiple lentigines syndrome
Muscular dystrophy - Duchenne type
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Mucopolysa- ccharidosis ii
Mucopolysa- ccharidosis vii
Mucolipidoses
MPS II
McArdle syndrome
more...
Diseases and disorders
(28)
Mucopolysa- ccharidosis vi
Mucocutaneous lymph node disease
Myotonia atrophica
Munchausens syndrome
Myxomatous mitral valve
Myxomatous mitral valve
Muscle fasciculation
Cytomegalovirus
Myxoma
Alpha-l-iduronidase deficiency
Mucous retention cyst
Megarectum
Mesangiocapillary glomerulonephritis
Joint stiffness
Dysostosis
Dwarfism
Medulloblastoma
Meningioma
Meningococcal
Malignant melanoma
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iv
Mucopolysa- ccharidosis, type I
Mucopolysa- ccharidosis ii
Mucopolysa- ccharidosis vii
Mucolipidoses
MPS II
Muscular dystrophy - Duchenne type
Lysosomal storage diseases
more...
Syndromes
Deformities
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis, type I
Mucopolysa- ccharidosis ii
Mucopolysa- ccharidosis vii
Munchausens syndrome
Multiple lentigines syndrome
Hydrolases
(8)
Iduronate sulfatase
Alpha-L iduronidase
N-acetylga- lactosamine-6-sulfate sulfatase
N-acetylga- lactosamine-6-sulfatase
Arylsulfatase B
Arylsulfatase B
N-acetylgl- ucosamine-6-sulfatase
Alpha-N-ac- etylglucosaminidase
Beta galactosidase
more...
Glycosaminoglycans
(9)
Chondroitin sulfate
Dermatan sulfate
Heparan sulfate
Keratan sulfate
Mucopolysaccharide
Mucopolysaccharide
Heparin
Heparinoid
Hyaluronan
Restylane
more...
Symptoms
(13)
Movement dysfunctional
Motormental retardation
Muscle function loss
Uncoordinated movement
Coarse facial features
Coarse facial features
Cloudy cornea
Hirsutism
Prognathism
Mental deterioration
Skeletal deformities
Muscle fasciculation
Joint stiffness
Short stature
more...
Signs and tests
(9)
Aortic insufficiency
Culture - skin
Hearing impairment
Hepatomegaly
Inguinal hernia
Inguinal hernia
Umbilical hernia
Urine dermatan sulfate
X-ray of the skeleton
Prognathism
more...
See also
(20)
Monorchism
Myocardial contusion
Enzyme
IVB
Sulfatase
Sulfatase
Midface trauma
Clouding
Anemia, macrocytic
Muscle glycogen phosphorylase
Mucinoses
Clouding of the cornea
Genetic counseling
Www.mpssociety.org
Enzyme replacement therapy
Short stature
Carbohydrate metabolism, inborn errors
Bone marrow transplantation
Idursulfase
Corneal
Autosomal recessive
more...
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