Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation

• Published in: European journal of paediatric neurology 2009-03, Vol.13 (2), p.191-193
• Main Authors: Zafeiriou, D.I, Lehmann-Horn, F, Vargiami, E, Teflioudi, E, Ververi, A, Jurkat-Rott, K
• Format: Article
• Language: English
• Subjects: Acetazolamide; Adult; CACNA1A gene; Calcium Channels - genetics; Child; Diarrhea; Diarrhea - genetics; Diarrhea - physiopathology; DNA Mutational Analysis; Episodic ataxia type 2; Female; Humans; Hyperhidrosis; Hyperhidrosis - genetics; Hyperhidrosis - physiopathology; Hypothermia - genetics; Hypothermia - physiopathology; Magnetic Resonance Imaging; Male; Migraine; Mutation; Neurology; Pediatrics; Spinocerebellar Ataxias - diagnosis; Spinocerebellar Ataxias - genetics; Spinocerebellar Ataxias - pathology; Spinocerebellar Ataxias - physiopathology
• ISSN: 1090-3798; 1532-2130
• DOI: 10.1016/j.ejpn.2008.02.011

Abstract Autosomal dominant episodic ataxia type 2 (EA2) results from mutations of the CACNA1A gene. We describe EA2 with unusual features in a father and daughter with a novel CACNA1A mutation coding for Y248C. Both patients showed severe cerebellar atrophy in MRI and clinical signs of progressive spinocerebellar atrophy type 6. Most disabling were the very frequent episodes of ataxia with migraine (with aura in the father and without aura in the daughter) and nystagmus in our patients. Additionally, they suffered from ictal hyperhidrosis with acute hypothermia of the extremities. Lastly, the father presented with interictal chronic diarrhea not associated to a known primary gastrointestinal disorder. Both ictal hyperhidrosis and interictal diarrhea ameliorated upon acetazolamide intake, the typical treatment for EA2. The significance of these findings is discussed and the phenotype correlated to previously reported cases.