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Neurological Sciences

, Volume 39, Issue 12, pp 2231–2233 | Cite as

Inaugural cognitive decline, late disease onset and novel STUB1 variants in SCAR16

  • José Gazulla
  • Silvia Izquierdo-Alvarez
  • Esther Sierra-Martínez
  • María Eugenia Marta-Moreno
  • Sara Alvarez
Letter to the Editor
  • 53 Downloads

Mutations in STUB1, on chromosome 16p13.3, have been associated with autosomal recessive spinocerebellar ataxia type 16 (SCAR16) [1] and found to cause ataxia and hypogonadism.

A 68-year-old woman experienced menarche at 12; afterwards, she had regular menses, gave birth to a girl, and had menopause at 47. At 54 years of age, progressively scarce spontaneous language, apathy and infantile behaviour developed, together with difficulty to perform calculations and domestic tasks. Four years later, unsteady gait developed and 6 years after, generalized involuntary movements appeared.

On examination, choreic movements affected the face, neck, trunk and extremities. Gait was wide-based and dysmetria was observed in the limbs. Horizontal nystagmus was present on lateral gaze and ocular pursuit was abnormal. An explosive dysarthria was noted.

Serial neuropsychological testing performed on four occasions over the last 9 years, using the Wisconsin Card Sorting Test, Boston Naming Test, Trail...

Notes

Compliance with ethical standards

Conflicts of interest

The authors declare that they have no conflict of interest.

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Copyright information

© Springer-Verlag Italia S.r.l., part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of NeurologyHospital Universitario Miguel ServetZaragozaSpain
  2. 2.Section of GeneticsHospital Universitario Miguel ServetZaragozaSpain
  3. 3.NIMGeneticsMadridSpain

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