Leukodystrophy, Metachromatic
"Leukodystrophy, Metachromatic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal recessive metabolic disease caused by a deficiency of CEREBROSIDE-SULFATASE leading to intralysosomal accumulation of cerebroside sulfate (SULFOGLYCOSPHINGOLIPIDS) in the nervous system and other organs. Pathological features include diffuse demyelination, and metachromatically-staining granules in many cell types such as the GLIAL CELLS. There are several allelic and nonallelic forms with a variety of neurological symptoms.
Descriptor ID |
D007966
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MeSH Number(s) |
C10.228.140.163.100.362.550 C10.228.140.163.100.435.825.850.500 C10.228.140.695.625.550 C10.228.518.625.550 C10.314.400.550 C16.320.565.189.362.550 C16.320.565.189.435.825.850.500 C16.320.565.398.641.803.925.500 C16.320.565.595.554.825.850.500 C18.452.132.100.362.550 C18.452.132.100.435.825.850.500 C18.452.584.687.803.925.500 C18.452.648.189.362.550 C18.452.648.189.435.825.850.500 C18.452.648.398.641.803.925.500 C18.452.648.595.554.825.850.500
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Concept/Terms |
Leukodystrophy, Metachromatic- Leukodystrophy, Metachromatic
- Leukodystrophies, Metachromatic
- Metachromatic Leukodystrophies
- Cerebral sclerosis, Diffuse, Metachromatic Form
- Sulfatide Lipidosis
- Lipidosis, Sulfatide
- Metachromatic Leukodystrophy
- Metachromatic Leukoencephalopathy
- Leukoencephalopathies, Metachromatic
- Leukoencephalopathy, Metachromatic
- Metachromatic Leukoencephalopathies
- Arylsulfatase A Deficiency Disease
- Cerebroside Sulphatase Deficiency Disease
Leukodystrophy, Metachromatic, Adult- Leukodystrophy, Metachromatic, Adult
- Metachromatic Leukodystrophy, Adult-Type
- Adult-Type Metachromatic Leukodystrophies
- Adult-Type Metachromatic Leukodystrophy
- Leukodystrophies, Adult-Type Metachromatic
- Leukodystrophy, Adult-Type Metachromatic
- Metachromatic Leukodystrophies, Adult-Type
- Metachromatic Leukodystrophy, Adult Type
- Metachromatic Leukodystrophy, Adult
- Adult Metachromatic Leukodystrophies
- Adult Metachromatic Leukodystrophy
- Leukodystrophies, Adult Metachromatic
- Leukodystrophy, Adult Metachromatic
- Metachromatic Leukodystrophies, Adult
Metachromatic Leukodystrophy, Infant- Metachromatic Leukodystrophy, Infant
- Infant Metachromatic Leukodystrophies
- Infant Metachromatic Leukodystrophy
- Metachromatic Leukodystrophies, Infant
- Metachromatic Leukodystrophy, Late Infantile
- Greenfield's Disease
- Greenfield Disease
- Metachromatic Leukodystrophy, Infant-Type
- Infant-Type Metachromatic Leukodystrophies
- Infant-Type Metachromatic Leukodystrophy
- Metachromatic Leukodystrophies, Infant-Type
- Metachromatic Leukodystrophy, Infant Type
Arylsulfatase A Deficiency- Arylsulfatase A Deficiency
- Arylsulfatase A Deficiencies
- Deficiencies, Arylsulfatase A
- Deficiency, Arylsulfatase A
- ARSA Deficiency
- ARSA Deficiencies
- Deficiencies, ARSA
- Deficiency, ARSA
- Cerebroside Sulfatase Deficiency
- Cerebroside Sulfatase Deficiencies
- Deficiencies, Cerebroside Sulfatase
- Deficiency, Cerebroside Sulfatase
- Sulfatase Deficiencies, Cerebroside
- Sulfatase Deficiency, Cerebroside
Leukodystrophy, Metachromatic, Juvenile- Leukodystrophy, Metachromatic, Juvenile
- Metachromatic Leukodystrophy, Juvenile-Type
- Juvenile-Type Metachromatic Leukodystrophies
- Juvenile-Type Metachromatic Leukodystrophy
- Leukodystrophies, Juvenile-Type Metachromatic
- Leukodystrophy, Juvenile-Type Metachromatic
- Metachromatic Leukodystrophies, Juvenile-Type
- Metachromatic Leukodystrophy, Juvenile Type
- Metachromatic Leukodystrophy, Juvenile
- Juvenile Metachromatic Leukodystrophies
- Juvenile Metachromatic Leukodystrophy
- Leukodystrophies, Juvenile Metachromatic
- Leukodystrophy, Juvenile Metachromatic
- Metachromatic Leukodystrophies, Juvenile
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Below are MeSH descriptors whose meaning is more general than "Leukodystrophy, Metachromatic".
- Diseases [C]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Brain Diseases [C10.228.140]
- Brain Diseases, Metabolic [C10.228.140.163]
- Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
- Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.163.100.362]
- Leukodystrophy, Metachromatic [C10.228.140.163.100.362.550]
- Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
- Sphingolipidoses [C10.228.140.163.100.435.825]
- Sulfatidosis [C10.228.140.163.100.435.825.850]
- Leukodystrophy, Metachromatic [C10.228.140.163.100.435.825.850.500]
- Leukoencephalopathies [C10.228.140.695]
- Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.695.625]
- Leukodystrophy, Metachromatic [C10.228.140.695.625.550]
- Leukoencephalopathies [C10.228.518]
- Hereditary Central Nervous System Demyelinating Diseases [C10.228.518.625]
- Leukodystrophy, Metachromatic [C10.228.518.625.550]
- Demyelinating Diseases [C10.314]
- Hereditary Central Nervous System Demyelinating Diseases [C10.314.400]
- Leukodystrophy, Metachromatic [C10.314.400.550]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Hereditary Central Nervous System Demyelinating Diseases [C16.320.565.189.362]
- Leukodystrophy, Metachromatic [C16.320.565.189.362.550]
- Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435]
- Sphingolipidoses [C16.320.565.189.435.825]
- Sulfatidosis [C16.320.565.189.435.825.850]
- Leukodystrophy, Metachromatic [C16.320.565.189.435.825.850.500]
- Lipid Metabolism, Inborn Errors [C16.320.565.398]
- Lipidoses [C16.320.565.398.641]
- Sphingolipidoses [C16.320.565.398.641.803]
- Sulfatidosis [C16.320.565.398.641.803.925]
- Leukodystrophy, Metachromatic [C16.320.565.398.641.803.925.500]
- Lysosomal Storage Diseases [C16.320.565.595]
- Lysosomal Storage Diseases, Nervous System [C16.320.565.595.554]
- Sphingolipidoses [C16.320.565.595.554.825]
- Sulfatidosis [C16.320.565.595.554.825.850]
- Leukodystrophy, Metachromatic [C16.320.565.595.554.825.850.500]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Hereditary Central Nervous System Demyelinating Diseases [C18.452.132.100.362]
- Leukodystrophy, Metachromatic [C18.452.132.100.362.550]
- Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435]
- Sphingolipidoses [C18.452.132.100.435.825]
- Sulfatidosis [C18.452.132.100.435.825.850]
- Leukodystrophy, Metachromatic [C18.452.132.100.435.825.850.500]
- Lipid Metabolism Disorders [C18.452.584]
- Lipidoses [C18.452.584.687]
- Sphingolipidoses [C18.452.584.687.803]
- Sulfatidosis [C18.452.584.687.803.925]
- Leukodystrophy, Metachromatic [C18.452.584.687.803.925.500]
- Metabolism, Inborn Errors [C18.452.648]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Hereditary Central Nervous System Demyelinating Diseases [C18.452.648.189.362]
- Leukodystrophy, Metachromatic [C18.452.648.189.362.550]
- Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435]
- Sphingolipidoses [C18.452.648.189.435.825]
- Sulfatidosis [C18.452.648.189.435.825.850]
- Leukodystrophy, Metachromatic [C18.452.648.189.435.825.850.500]
- Lipid Metabolism, Inborn Errors [C18.452.648.398]
- Lipidoses [C18.452.648.398.641]
- Sphingolipidoses [C18.452.648.398.641.803]
- Sulfatidosis [C18.452.648.398.641.803.925]
- Leukodystrophy, Metachromatic [C18.452.648.398.641.803.925.500]
- Lysosomal Storage Diseases [C18.452.648.595]
- Lysosomal Storage Diseases, Nervous System [C18.452.648.595.554]
- Sphingolipidoses [C18.452.648.595.554.825]
- Sulfatidosis [C18.452.648.595.554.825.850]
- Leukodystrophy, Metachromatic [C18.452.648.595.554.825.850.500]
Below are MeSH descriptors whose meaning is more specific than "Leukodystrophy, Metachromatic".
This graph shows the total number of publications written about "Leukodystrophy, Metachromatic" by people in UAMS Profiles by year, and whether "Leukodystrophy, Metachromatic" was a major or minor topic of these publications.
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Below are the most recent publications written about "Leukodystrophy, Metachromatic" by people in Profiles over the past ten years.
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