Fahr’s syndrome and idiopathic hypoparathyroidism: A case report

Author:

Marinkovic Dejan1,Dragovic Tamara2,Kikovic Sasa1,Kuzmic-Jankovic Snezana1,Djuran Zorana1,Hajdukovic Zoran2

Affiliation:

1. Military Medical Academy, Clinic for Endocrinology, Belgrade

2. Military Medical Academy, Clinic for Endocrinology, Belgrade + University of Defence, Faculty of Medicine of the Military Medical Academy, Belgrade

Abstract

Introduction. Fahr?s syndrome is a rare, slowly progressive, neurodegenerative disorder, characterised by extensive, bilateral, and symmetrical basal ganglia calcification. It is associated with neuropsychiatric manifestations and gradually progressive cognitive impairment. Fahr's syndrome is the secondary form of brain calcification that is caused by various metabolic, infectious, or degenerative diseases. Case report. We presented a middle-aged male with Fahr's syndrome due to primary idiopathic hypoparathyroidism. Clinical diagnosis was based on signs and symptoms of hypocalcemia, progressive neuropsychiatric illnesses, laboratory evidence of hypoparathyroidism, and radiological signs of calcifications in the basal ganglia. The patient improved after only a few days of intravenous rehydration and calcium substitution, followed by oral supplemental calcitriol. Conclusion. Timely recognition of idiopathic and iatrogenic hypoparathyroidism allows appropriate treatment that can prevent the development and clinical manifestations of Fahr?s syndrome and potentially slow its progression.

Publisher

National Library of Serbia

Subject

Pharmacology (medical),General Medicine

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Síndrome de Fahr - A propósito de un caso;Galicia Clínica;2022

2. Signes neuropsychologiques chez l’enfant : penser au syndrome de Fahr;Neuropsychiatrie de l'Enfance et de l'Adolescence;2019-03

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