Huntington disease

Case contributed by Dr Gabrielle Matta

Presentation

The patient exhibited upper limb choreic and dystonic movements. There were subtle facial movements, motor impersistence of the tongue and lower limb toe chorea. Gait was unsteady and wide-based. There was a recent psychiatric admission due to presentation with a persecutory delusion that his father had locked up his (imaginary) daughter.

Patient Data

Age: 40
Gender: Male
MRI

Marked atrophy of the caudate nucleus and putamen are noted. No restricted diffusion or susceptibility artefact. No enhancing lesions on the post contrast study.

There is atrophy of the frontoparietal and occipital lobes. No atrophy of the cerebellum.

Photo

NUCOG

Neuropsychiatry Unit Cognitive Assessment Tool (NUCOG) performed on this patient.

Scores across most domains are more than two standard deviations below normal.

Nuclear medicine

Cerebral Perfusion Study

Reduced uptake is seen in the heads of the caudate nuclei, worse on the left side. In addition, hypoperfusion is seen in in the parietal lobes particularly in the left superior parietal lobe. The perfusion is also mildly reduced in the mesial temporal lobes.
 

MRI

MRI - Frontal horn width to intercaudate ratio

This frontal horn width to intercaudate ratio (FH/CC) is demonstrated in this image taken from the above patient.

FH/CC = 3.33/2.44

= 1.36 (normal 2.2 - 2.6)

Case Discussion

This patient presented with moderate stage symptoms (motor, cognitive, psychiatric). Gene testing demonstrated HTT allele I size 18, allele II size 46 (normal range <36). The MRI brain shows significant global atrophy. The caudate heads are flat and putamen is atrophied.

These are typical and characteristic appearances of Huntington's disease

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Case information

rID: 43391
Case created: 8th Mar 2016
Last edited: 26th Apr 2016
Inclusion in quiz mode: Included

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