Considering Huntington's Disease and Neuroacanthocytosis in the Differential Diagnosis of Senile Chorea

Elmali A. D., Gunduz A., Baslar Z., Ertan F. S.

TURKISH JOURNAL OF NEUROLOGY, cilt.21, sa.3, ss.119-123, 2015 (ESCI) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 21 Sayı: 3
  • Basım Tarihi: 2015
  • Doi Numarası: 10.4274/tnd.34545
  • Dergi Adı: TURKISH JOURNAL OF NEUROLOGY
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus
  • Sayfa Sayıları: ss.119-123
  • İstanbul Üniversitesi Adresli: Evet

Özet

Sporadic chorea that presents after the age of 50 years is called "senile chorea". Senile chorea is a rare entity with a wide differential diagnosis list. Causes of senile chorea include vascular and metabolic diseases, adverse events related to medications, hematologic and immune system diseases, genetic and sporadic neurodegenerative syndromes, and paraneoplastic disorders. Although the most common etiologies are vascular and metabolic disorders, neuroacanthocytosis, Wilson's and Huntington's disease are included in the differential diagnosis.