Leukodystrophy, Metachromatic [metachromatická leukodystrofie]
- Terms
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deficit arylsulfatázy A
deficit cerebrosidsulfatázy
Greenfieldova nemoc
leukodystrofie metachromatická
metachromatická leukodystrofie adultní forma
metachromatická leukodystrofie juvenilní
metachromatická leukodystrofie pozdní infantilní
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ARSA Deficiency
Arylsulfatase A Deficiency
Arylsulfatase A Deficiency Disease
Cerebral sclerosis, Diffuse, Metachromatic Form
Cerebroside Sulfatase Deficiency
Cerebroside Sulphatase Deficiency Disease
Greenfield Disease
Greenfield's Disease
Leukodystrophy, Metachromatic, Adult
Leukodystrophy, Metachromatic, Juvenile
Metachromatic Leukodystrophy
Metachromatic Leukodystrophy, Adult
Metachromatic Leukodystrophy, Adult-Type
Metachromatic Leukodystrophy, Infant
Metachromatic Leukodystrophy, Infant-Type
Metachromatic Leukodystrophy, Juvenile
Metachromatic Leukodystrophy, Juvenile-Type
Metachromatic Leukodystrophy, Late Infantile
Metachromatic Leukoencephalopathy
Sulfatide Lipidosis
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.
- DUI
- D007966 MeSH Browser
- CUI
- M0012416
- History note
- 1974
- Public note
- 1974
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 2
- CO
- complications 2
- DI
- diagnosis 13
- DG
- diagnostic imaging 1
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology 1
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology 7
- GE
- genetics 7
- HI
- history
- IM
- immunology
- ME
- metabolism 3
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 3
- PP
- physiopathology 3
- PC
- prevention & control
- PX
- psychology 1
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 5
- UR
- urine 2
- VE
- veterinary
- VI
- virology
Cerebral Sclerosis, Diffuse, Scholz Type Disease MeSH Browser
Combined Saposin Deficiency Disease MeSH Browser
Metachromatic Leukodystrophy due to Saposin B Deficiency Disease MeSH Browser
Metachromatic Leukodystrophy, Adult-Onset, with Normal Arylsulfatase A Disease MeSH Browser
Pseudoarylsulfatase A Deficiency Disease MeSH Browser