familial Infantile convulsions and paroxysmal choreoathetosis
A hereditary autosomal dominant disorder characterized by afebrile seizures occurring between 3 and 12 months of age. Paroxysmal choreoathetosis is a disorder of involuntary movements characterized by attacks that occur spontaneously or are induced by a variety of stimuli. Mutations in the PRRT2 gene have been identified. OMIM: 602066
Also Known As:
Infantile convulsions and paroxysmal choreoathetosis, familial; Convulsions, infantile, with paroxysmal choreoathetosis, familial; ICCA Infantile convulsions and choreoathetosis
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