A Rare Neurological Disorder Characterized By Atypical Findings: Fahr's Disease
Öz
Fahr’s
disease (bilateral striopallidodentate calcinosis) is a rare disease
characterized by neurodegenerative disorders and accompanied by calcinosis in
cerebellum, thalamus and basal ganglia which is caused by calcium and
phosphorus metabolism disorders. The accumulation of calcium and various
minerals in parenchyma can be shown by cranial tomography. Although the
etiology of this disease is not known for certain, disorders of calcium
metabolism, toxins, infections, genetic factors, hypoparathyroidism, and
pseudohypoparathyroidism have been shown among the causes. In this article we
presented three patients who have admitted to the emergency department with the
same neurological symptoms, and diagnosed with Fahr’s disease that is
considered secondary to hypoparathyroidism due to different etiologic factors.
Bilateral caudate nucleus and cerebellar calcifications have been determined in
computed cerebral topographies of our cases. Fahr’s disease must be considered
in the differential diagnosis of patients who have sudden onset
neuropsychiatric symptoms, calcium metabolism disorders and/or develop
unexplainedneurological symptoms that reason cannot be found.
Anahtar Kelimeler
Kaynakça
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Ayrıntılar
Birincil Dil
Türkçe
Konular
-
Bölüm
Olgu Sunumu
Yayımlanma Tarihi
26 Mayıs 2017
Gönderilme Tarihi
3 Ağustos 2016
Kabul Tarihi
1 Eylül 2016
Yayımlandığı Sayı
Yıl 2017 Cilt: 31 Sayı: 1