Catalog

McLeod syndrome

No MMS code

Link to WHO Definition

McLeod syndrome – http://id.who.int/icd/entity/463702616

An X linked disorder of neuroacanthocytosis that is caused by mutations in the XK gene coding for the Kell antigens red blood cells. Characterized by degeneration of the caudate and putamen leading to progressive chorea, peripheral neuropathy, and myopathy with increase in serum creatine kinase level.