Publication:
Fahr’s Disease: A Rare Neurological Disorder Associated with Secondary Cause

creativeworkseries.issn1812-2027
dc.contributor.authorBhatta, Y
dc.contributor.authorMalla, A
dc.contributor.authorChaurasiya, AK
dc.contributor.authorPokharel, BR
dc.date.accessioned2026-01-06T07:16:41Z
dc.date.available2026-01-06T07:16:41Z
dc.date.issued2023
dc.descriptionBhatta Y, Malla A, Chaurasiya AK, Pokharel BR Department of Neurology Nepal Mediciti Hospital Bhaisepati, Lalitpur, Nepal
dc.description.abstractABSTRACT Fahr’s disease is characterized by idiopathic bilateral deposition of calcium in the striopallidodentate area. We are presenting 83-year-old female, who failed responding while having lunch around 10 AM soon after she lost consciousness for an hour. It was associated with difficulty in walking, mood disturbances, fatigability, blurring of vision and occasional dizziness since past 4 months. Her neurological examination revealed Parkinsonian features. Her computed tomography of head report showed bilateral, symmetrical, large area of calcification over the basal ganglia, the thalamus and the cerebellum. To rule out the seizure disorder we have done an electroencephalogram and some laboratory test including calcium, Phosphorus, Parathyroid hormone and magnesium, vitamin D which were suggestive of Fahr’s disease. KEY WORDS Basal ganglia diseases, Calcinosis, Fahr’s disease, Neurological disorder
dc.identifier.urihttps://hdl.handle.net/20.500.14572/4084
dc.language.isoen_US
dc.publisherKathmandu University
dc.subjectBasal ganglia diseases
dc.subjectCalcinosis
dc.subjectFahr’s disease
dc.subjectNeurological disorder
dc.titleFahr’s Disease: A Rare Neurological Disorder Associated with Secondary Cause
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage339
oaire.citation.startPage337
relation.isJournalIssueOfPublicationd5d9c4fe-93e1-4b2c-8881-0edc27057501
relation.isJournalIssueOfPublication.latestForDiscoveryd5d9c4fe-93e1-4b2c-8881-0edc27057501
relation.isJournalOfPublicationa782b7ff-cf89-4178-ad1c-11ed89cfe1bd

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