Ct Diagnosis of Fahr's Disease, A Case Report
<p>Fahr's disease is a rare inherited or sporadic neurological disorder with a prevalence of <1/1,000,000, with a higher incidence reported among males and a typical age of onset in the 4th-6th 3rd-5th decade of life.</p><p>Fahr's disease, or idiopathic striopallidoden...
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Imaging Journal of Clinical and Medical Sciences - Peertechz Publications,
2018-04-19.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | peertech__10_17352_2455-8702_000038 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Antonio Gligorievski |e author |
245 | 0 | 0 | |a Ct Diagnosis of Fahr's Disease, A Case Report |
260 | |b Imaging Journal of Clinical and Medical Sciences - Peertechz Publications, |c 2018-04-19. | ||
520 | |a <p>Fahr's disease is a rare inherited or sporadic neurological disorder with a prevalence of <1/1,000,000, with a higher incidence reported among males and a typical age of onset in the 4th-6th 3rd-5th decade of life.</p><p>Fahr's disease, or idiopathic striopallidodentate calcinosis, or idiopathic basal ganglia calcification is a rare clinical entity characterized by bilateral and symmetrical intracerebral calcifications of the basal ganglia, thalamus, dentate nucleus and centrum semiovale in the absence of any metabolic abnormality including hypoparathyroidism.<br></p> | ||
540 | |a Copyright © Antonio Gligorievski et al. | ||
546 | |a en | ||
655 | 7 | |a Case Report |2 local | |
856 | 4 | 1 | |u https://doi.org/10.17352/2455-8702.000038 |z Connect to this object online. |