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Metachromatic leukodystrophy

MONDO:0018868

A rare lysosomal storage disorder characterized by intralysosomal accumulation of sulfatides in various tissues, leading to progressive deterioration of motor and neurocognitive function.

Also known as: MLD, arylsulfatase A deficiency

26 clinical trials for this condition and its sub-types.

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Sub-types

Metachromatic leukodystrophy, juvenile form (2) Metachromatic leukodystrophy, late infantile form (2) Metachromatic leukodystrophy, adult form (0) Metachromatic leukodystrophy due to saposin B deficiency (0)

Broader categories

Dementia (698) Disease (680) Psychiatric disorder (435) Cognitive disorder (433) Metabolic disease (233) Nervous system disorder (231) Inherited lipid metabolism disorder (189) Hereditary disease (176) Neurodegenerative disease (171) Peripheral nervous system disorder (114)
Trials to join now! 12 Not yet finished but already full! 4 Completed 9 Terminated 1
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