Journal of Pediatric Neurology 2009; 07(03): 329-331
DOI: 10.3233/JPN-2009-0306
Case Report
Georg Thieme Verlag KG Stuttgart – New York

Vitiligo with spastic paraparesis: A rare neurocutaneous syndrome

Subinay Mandal
a   Department of Pediatrics, Bankura Sammilani Medical College and Hospital, Bankura, West Bengal, India
,
Debashis Bid
a   Department of Pediatrics, Bankura Sammilani Medical College and Hospital, Bankura, West Bengal, India
› Author Affiliations

Subject Editor:
Further Information

Publication History

08 September 2008

13 December 2008

Publication Date:
30 July 2015 (online)

Abstract

Hereditary spastic paraparesis/familial spastic paraparesis is a group of clinically and genetically diverse disorders characterized by progressive usually severe, lower extremity weakness and spasticity. Vitiligo with spastic paraparesis, a disorder of hereditary spastic paraparesis group, is a rare neurocutaneous syndrome. Herein, we report a case of vitiligo with spastic paraparesis with a family history of similar type of disease in another sib, in a family of non-consanguineous marriage.