Concept information
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Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
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Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
...
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
...
Metabolic Diseases
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Término preferido
Sialic Acid Storage Disease
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Tipo
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mesh:Descriptor
Definición
- Autosomal recessive neurodegenerative disorders caused by lysosomal membrane transport defects that result in accumulation of free sialic acid (N-ACETYLNEURAMINIC ACID) within the lysosomes. The two main clinical phenotypes, which are allelic variants of the SLC17A5 gene, are ISSD, a severe infantile form, or Salla disease, a slowly progressive adult form, named for the geographic area in Finland where the kindred first studied resided.
Concepto genérico
Etiquetas alternativas
- Sialuria
En otras lenguas
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francés
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Anomalie du stockage en acide sialique
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Maladie de la surcharge en acide sialique
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Maladie de surcharge en acide sialique libre (SSD)
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Sialurie
URI
http://data.loterre.fr/ark:/67375/JVR-NB4HZCPM-Q
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