Flexion cervical spine MRI in Hirayama disease showing expansion of the dural venous plexus with presumed chronic ischaemic damage preferentially involving.

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 Hirayama Disease.  Aka Juvenile Muscular Atrophy of the Distal Upper Extremity  Rare disease that affects predominantly males in their 2 nd or early.
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Imaging studies in a patient with a distractive flexion injury of the cervical spine. (A) This lateral radiographic view demonstrates anterior subluxation.
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The MR scan of brain of our case vignette patient showing significant occipital lobe atrophy (especially left sided) with parietal lobe involvement as.
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Case one: (A and B) Right and left colour fundus photographs of the optic nerve head showing small crowded discs with anomalous branching of the blood.
Photograph of the legs of a patient with inherited erythromelalgia, showing erythema to the level of the mid-calf. Photograph of the legs of a patient.
MRI scans show coronal sections of the brain and right hippocampus at baseline, 9 months, 2 years (when he was diagnosed with mild cognitive impairment)
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Flexion cervical spine MRI in Hirayama disease showing expansion of the dural venous plexus with presumed chronic ischaemic damage preferentially involving.
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Erdheim–Chester disease.
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This 46-year-old man presented with a 20-year history of progressive distal wasting and weakness of the right hand and forearm muscles. This 46-year-old.
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MR scans of brain and spine: (A) sagittal T2 image showing signal change in the posterior spinal cord between C3 and T6. MR scans of brain and spine: (A)
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Flexion cervical spine MRI in Hirayama disease showing expansion of the dural venous plexus with presumed chronic ischaemic damage preferentially involving the anterior horn cells supplying the distal arm. Flexion cervical spine MRI in Hirayama disease showing expansion of the dural venous plexus with presumed chronic ischaemic damage preferentially involving the anterior horn cells supplying the distal arm. Martin R Turner, and Kevin Talbot Pract Neurol 2013;13:153-164 ©2013 by BMJ Publishing Group Ltd