A case of Fahr’s disease presenting with seizures
Author(s) -
Cihan Bedel,
Goker Coskun
Publication year - 2018
Publication title -
the annals of clinical and analytical medicine
Language(s) - English
Resource type - Journals
ISSN - 2667-663X
DOI - 10.4328/jcam.5687
Subject(s) - epilepsy , medicine , pediatrics , psychiatry
DOI: 10.4328/JCAM.5687 Received: 14.01.2018 Accepted: 14.02.2018 Publihed Online: 16.02.2018 Printed: 01.05.2018 J Clin Anal Med 2018;9(3): 251-3 Corresponding Author: Cihan Bedel, Acil Tıp ABD, Antalya Eğitim ve Araştırma Hastanesi, Antalya, Turkey. GSM: +905075641254 E-Mail: cihanbedel@hotmail.com Abstract Fahr’s disease is a rare idiopathic bilateral and symmetrical calcification of the basal ganglia, thalami, subcortical hemispheric white matter and deep cerebellar nuclei. We report an unusual case of Fahr’s disease in a 53-year-old man who presented with generalized seizure in our emergency department. Based on clinical, radiological and endocrinological appearance, the patient was diagnosed with Fahr’s disease associated with hypoparathyroidism. Parenteral calcium and calcitriol supplementation were given in the emergency department. The clinical outcome was favorable after the treatment. Our case illustrates that Fahr’s disease, though rarely seen, has to be considered in a patient with convulsive state associated with calcifications of the basal ganglia.
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