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Hurler Disease
Hurler disease
Overview
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Related in the Kosmos
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Skin conditions resulting from errors in metabolism
Mucolipidosis I
Fucosidosis
Niemann Pick disease
Hunter syndrome
Gaucher disease
Autosomal recessive disorders
(14)
Beta-mannosidosis
Alpha-mannosidosis
Salla disease
Scheie syndrome
Aspartylgl- ucosaminuria
Aspartylgl- ucosaminuria
Mucolipidosis
Mucolipidosis type IV
Gangliosidosis
Sanfilippo syndrome
Tay Sachs disease
Sandhoff disease
Fucosidosis
Niemann Pick disease
Gaucher disease
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Genetic disorders
(18)
Hyperimmunoglobulin E syndrome
Pseudo-Hurler polydystrophy
Galactosialidosis
Gangliosidosis gm1
Beta-mannosidosis
Beta-mannosidosis
Salla disease
Scheie syndrome
Aspartylgl- ucosaminuria
Mucolipidosis
Mucolipidosis type IV
Fucosidosis
Gangliosidosis
Sanfilippo syndrome
Tay Sachs disease
Sandhoff disease
Niemann Pick disease
Hunter syndrome
Gaucher disease
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Hepatology
Hepatosplenomegaly
Gaucher disease
Syndromes
Horners syndrome
Hyperimmunoglobulin E syndrome
Sanfilippo syndrome
Hunter syndrome
Lysosomal storage diseases
(39)
Glycoproteinosis
I-cell disease
Lysosomal storage disease
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
Galactosialidosis
Gangliosidosis
Gangliosidosis gm1
Gaucher disease
Glycogen storage disease type II
Hunter syndrome
Krabbe disease
Lipid storage disorder
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis I
Mucolipidosis type IV
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Scheie syndrome
Schindler disease
Sly syndrome
Tay Sachs disease
Wolman disease
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Diseases and disorders
(33)
Hypochondriacal neurosis
Hutchinson incisors
Hyperchylo- micronemia
Hypolipoproteinemia
Horizontal nystagmus
Horizontal nystagmus
Hypercalciuria
Maroteaux-Lamy syndrome
Dwarfism
Leukemias
Mental retardation
Iodine deficiency
Myelofibrosis
Hyperimmunoglobulin E syndrome
Horners syndrome
Beta-mannosidosis
Glycoproteinosis
Lysosomal storage diseases
Salla disease
Galactosialidosis
Scheie syndrome
Aspartylgl- ucosaminuria
Mucolipidosis
Mucolipidosis type IV
Mucolipidosis I
Gangliosidosis gm1
Fucosidosis
Gangliosidosis
Sanfilippo syndrome
Tay Sachs disease
Sandhoff disease
Niemann Pick disease
Hunter syndrome
Gaucher disease
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Hematology
Hyperviscosity.
Bone marrow transplantation
Hypolipoproteinemia
Leukemias
Gaucher disease
Symptoms
Hypertrophic scar
Coarse facial features
Deafness
Low nasal bridge
Skeletal deformities
Mental retardation
Definition
MPS I S (Scheie syndrome)
MPS II, Hunter syndrome
MPS III (Sanfilippo syndrome)
MPS IV (Morquio syndrome)
Metabolism
See also
(20)
Human artificial chromosome
Hyperparat- hyroidism, secondary
Hypertrigl- yceridemia
Alpha-L iduronidase
Hurling
Hurling
Vietnam
Electrocardiography
Enzyme
Genetic counseling
Www.mpssociety.ca
Www.mpssoc- iety.co.uk
Www.mpssociety.org
Lysosomal enzymes
Enzyme replacement
Facies
Glycosaminoglycans
Mucopolysaccharides
Autosomal recessive
Diseases Database
Umbilical cord blood
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