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Morquio
Morquio
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Related in the Kosmos
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Lysosomal storage diseases
(39)
Gangliosidosis
Hunter syndrome
Lysosomal storage disease
Mucolipidoses
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis, type I
Sly syndrome
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
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
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Autosomal recessive disorders
(8)
Ellis-van creveld syndrome
Isovaleric acidemia
Mucopolysa- ccharidosis iii
Mucolipidoses
Mucopolysa- ccharidosis, type I
Mucopolysa- ccharidosis, type I
Mucopolysa- ccharidosis
Sly syndrome
Gangliosidosis
more...
Skin conditions resulting from errors in metabolism
Mucopolysa- ccharidosis, type I
Hunter syndrome
Genetic disorders
(15)
Myoclonic Epilepsy with Ragged Red Fibers
Multiple lentigines syndrome
Achondroplasia
Osteogenesis imperfecta
Muscular dystrophy
Muscular dystrophy
Spondyloepiphyseal dysplasia
Mucopolysa- ccharidosis iii
Mucolipidoses
Mucopolysa- ccharidosis, type I
Mucopolysa- ccharidosis
Sly syndrome
Hunter syndrome
Ellis-van creveld syndrome
Isovaleric acidemia
Gangliosidosis
more...
Rare diseases
Mucopolysa- ccharidosis iii
Sly syndrome
Isovaleric acidemia
Gangliosidosis
Diseases and disorders
(28)
Morquio syndrome type b
Mucocutaneous lymph node disease
Myotonia atrophica
Munchausens syndrome
Myxomatous mitral valve
Myxomatous mitral valve
Muscle fasciculation
Infectious mononucleosis
Myxoma
Maroteaux-Lamy syndrome
Dwarfism
Pectus carinatum
Curvature of the spine
Macrocephaly
Iodine deficiency
Dysostosis
Skeletal dysplasia
Mucopolysa- ccharidosis iii
Mucolipidoses
Mucopolysa- ccharidosis, type I
Mucopolysa- ccharidosis
Sly syndrome
Hunter syndrome
Ellis-van creveld syndrome
Achondroplasia
Osteogenesis imperfecta
Muscular dystrophy
Spondyloepiphyseal dysplasia
Gangliosidosis
more...
Glycosaminoglycans
(9)
Chondroitin sulfate
Keratan sulfate
Mucopolysaccharides
Dermatan sulfate
Heparan sulfate
Heparan sulfate
Heparin
Heparinoid
Hyaluronan
Restylane
more...
Amino sugars
Acetylgalactosamine
Galactosamine
Glycosaminoglycans
Symptoms
(12)
Movement dysfunctional
Motormental retardation
Muscle function loss
Uncoordinated movement
Hypermobile joints
Hypermobile joints
Widely spaced teeth
Coarse facial features
Cloudy cornea
Skeletal deformities
Missing teeth
Muscle fasciculation
Short stature
more...
Hydrolases
GALNS
N-acetylga- lactosamine-6-sulfatase
Beta galactosidase
Iduronidase
Naglazyme
Alpha-N-ac- etylglucosaminidase
Signs and tests
Aortic insufficiency
Blood culture
Hearing test
Inguinal hernia
Liver enlargement
Slit lamp
X-rays
Definition
MPS I H (Hurler syndrome)
MPS I S (Scheie syndrome)
MPS II, Hunter syndrome
MPS III (Sanfilippo syndrome)
See also
(20)
Monorchism
Myocardial contusion
IVB
Sulfatase
Heparan sulfamidase
Heparan sulfamidase
Chondroitin 6-sulfate
Short stature
Galactose 6-sulfatase
Enzyme
Genetic counseling
Heart failure
Www.mpssociety.org
BioMarin Pharmaceutical
Maxwell Kane
Brailsford
Enzyme replacement therapy
Autosomal
Kyphosis
Ligamentous laxity
Osseous
more...
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