Repetitive Daily Blindness with Hemiplegic Migraine and SCN1A Mutations

Abstract

Two novel SCN1A mutations are identified in two unrelated families with familial hemiplegic migraine and a unique phenotype of elicited repetitive daily blindness, in a report from Hopital Lariboisiere, and other centers in Paris, France, and Geneva, Switzerland.

Keywords

• familial hemiplegic migraine
• visual symptoms
• electroretinogram