Condition
Leukodystrophy, Globoid Cell
Neurology
Overview
An autosomal recessive metabolic disorder caused by a deficiency of GALACTOSYLCERAMIDASE leading to intralysosomal accumulation of galactolipids such as GALACTOSYLCERAMIDES and PSYCHOSINE. It is characterized by demyelination associated with large multinucleated globoid cells, predominantly involving the white matter of the central nervous system. The loss of MYELIN disrupts normal conduction of nerve impulses.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Leukodystrophy, Globoid Cell
- Topic type
- Condition
- Category
- Neurology
- MeSH classification
- C10.228.140.163.100.362.500|C10.228.140.163.100.435.825.590|C10.228.140.695.625.500|C10.314.400.500|C16.320.565.189.362.500|C16.320.565.189.435.825.590|C16.320.565.398.641.803.585|C16.320.565.595.554.825.590|C18.452.132.100.362.500|C18.452.132.100.435.825.590|C18.452.584.563.641.803.585|C18.452.648.189.362.500|C18.452.648.189.435.825.590|C18.452.648.398.641.803.585|C18.452.648.595.554.825.590
Preparing for an appointment about Leukodystrophy, Globoid Cell
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- Write down your symptoms and when they started.
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- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.