<i>FGF14</i>‐related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9
Julie Piarroux, Florence Riant, Véronique Humbertclaude, Ganaëlle Remérand, Jessica Hadjadj, F Rejou, Christine Coubes, Lucile Pinson, Pierre Meyer, Agathe Roubertie
Abstract
We report four patients from two families who presented attacks of childhood-onset episodic ataxia associated with pathogenic mutations in the FGF14 gene. Attacks were triggered by fever, lasted several days, and had variable frequencies. Nystagmus and/or postural tremor and/or learning disabilities were noticed in individuals harboring FGF14 mutation with or without episodic ataxia. These cases and literature data delineate the FGF14-mutation-related episodic ataxia phenotype: wide range of age at onset (from childhood to adulthood), variable durations and frequencies, triggering factors including fever, and association to chronic symptoms. We propose to add FGF14-related episodic ataxia to the list of primary episodic ataxia as Episodic Ataxia type 9.