XK-related neurodegenerative disease
MONDO:0018945A form of neuroacanthocytosis and is characterized clinically by a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx antigen and by weak expression of the Kell antigens.
Also known as: MLS, McLeod neuroacanthocytosis syndrome, McLeod syndrome, X-linked McLeod syndrome, XK disease, MCLDS
12 clinical trials for this condition and its sub-types, 0 tagged with XK-related neurodegenerative disease itself.
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