Corpus ID: 16013029

Fahr’s disease with epilepsy, deafness, schizophreniform psychosis and autoimmune polymyositis: a case report

@inproceedings{Viteva2016FahrsDW,
  title={Fahr’s disease with epilepsy, deafness, schizophreniform psychosis and autoimmune polymyositis: a case report},
  author={Ekaterina Ivanova Viteva and Albena A. Djurkova},
  year={2016}
}
Fahr’s disease is a rare sporadic or inherited neurodegenerative disorder characterized by symmetrical bilateral calcifications in the basal ganglia and some other brain structures – dentate nucleus, thalamus, cerebral cortex, subcortical white matter, and hippocampus. We report a patient with Fahr’s disease who has been monitored for 11 years and is interesting for the clinical practice with the following particular features: 1. The patient fulfills the Fahr’s disease criteria with the… Expand
Fahr's Syndrome
Article info: Received: 23 June 2018 Revised: 11 August 2018 Accepted: 05 September 2018

References

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Familial idiopathic basal ganglia calcification (Fahr’s disease)
TLDR
Fahr’s disease should be considered in the differential diagnosis of psychiatric symptoms, particularly when associated with movement disorder, and should be differentiated from other conditions that can cause intracranial calcification. Expand
Fahr’s syndrome: literature review of current evidence
TLDR
Disease is as yet incurable but management and treatment strategies mainly focus on symptomatic relief and eradication of causative factors; however certain evidence is present to suggest that early diagnosis and treatment can reverse the calcification process leading to complete recovery of mental functions. Expand
Fahr's disease: a very rare cause of epilepsy.
TLDR
A case of Fahr's disease, who presented with complex partial seizure and behavioral abnormalities, and the cause of seizure was found to be bilateral calcification of cerebellum, basal ganglia and thalamus, due to abnormal calcium and phosphate metabolism. Expand
Fahr’s syndrome presenting with pure and progressive presenile dementia
TLDR
The clinical and radiological features of the patient point to this uncommon form of dementia, a 50-year-old woman with progressive dementia but neither extrapyramidal symptoms nor a metabolic disorder. Expand
[Neuropsychological and neurophysiological features of Fahr's disease].
TLDR
The pathogenesis of cognitive and motor changes in Fahr's disease is based in a dysfunction of cortico basal connections and their interhemispheric relations, which defines a subcortical dementia secondary to mineral deposits in subCortical structures. Expand
Fahr's Disease: A Case Report
TLDR
This rare case of idiopathic Fahr's disease in a child, which has never been reported in Indian literature has been brought out to highlight this unusual condition and its differentiation from the commoner Fahr’s syndrome. Expand
A case of psychosis due to Fahr's syndrome and response to behavioral disturbances with risperidone and oxcarbazepine
Calcification of basal ganglia or Fahr's syndrome is a rare disease characterized by bilateral and symmetrical intracranial deposition of calcium mainly in cerebral basal ganglia. Motor andExpand
Psychosis revealing familial idiopathic basal ganglia calcification.
TLDR
Only brain imaging, followed by an extensive etiological assessment, allows for diagnosis of familial idiopathic basal ganglia calcification (IBGC), a rare disorder of brain calcifications responsive to antipsychotic drugs. Expand
[Value of EEG in parathyroid gland disorders and/or symmetrical calcinosis of the basal ganglia (Fahr syndrome). Review of the literature with personal cases].
We evaluated the diagnostic value of EEG tracings in cases of non-arteriosclerotic symmetrical calcification of the basal ganglia (Fahr's syndrome). The group of 41 tracings was composed of probandsExpand
Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease).
TLDR
A multigenerational family with dominantly inherited IBGC is identified and, in 24 members of this family, a whole-genome scan is performed using polymorphic microsatellite markers to identify the first chromosomal locus for this disorder (IBGC1). Expand
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