Annals of Indian Academy of Neurology (Jan 2016)

Clinical and MRI findings of cerebellar agenesis in two living adult patients

  • Fazil Mustafa Gelal,
  • Tugce Ozlem Kalayci,
  • Mehmet Celebisoy,
  • Levent Karakas,
  • Hulya Erdogan Akkurt,
  • Feray Koc

DOI
https://doi.org/10.4103/0972-2327.160054
Journal volume & issue
Vol. 19, no. 2
pp. 255 – 257

Abstract

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Cerebellar agenesis (CA) is an extremely rare entity. We present two adult patients with CA. The 61-year-old man had ataxia, dysarthria, abnormalities in cerebellar tests, severe cognitive impairment, and moderate mental retardation. The 26-year-old woman had dysmetria, dysdiadochokinesia, and dysarthria as well as mild cognitive impairment and mild mental retardation. Magnetic resonance imaging (MRI) showed complete absence of the cerebellum with small residual vermis. Brainstem was hypoplastic and structures above tentorium were normal. Supratentorial white matter bundles were unaffected in diffusion tensor tractography. Only few adult patients with CA have so far been published. These cases show that patients with CA present with a variety of developmental, clinical, and mental abnormalities; and emphasize the role of the cerebellum in normal motor, language, and mental development.

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