Familial idiopathic basal ganglia calcification (Fahr's disease)
AA Mufaddel, GA Al-Hassani - Neurosciences Journal, 2014 - nsj.org.sa
Familial idiopathic basal ganglia calcification (Fahr's disease) is a rare neurodegenerative
disorder characterized by symmetrical and bilateral calcification of the basal ganglia …
disorder characterized by symmetrical and bilateral calcification of the basal ganglia …
Fahr's syndrome and clinical correlation: a case series and literature review
M Pistacchi, M Gioulis, F Sanson, SZ Marsala - Folia neuropathologica, 2016 - termedia.pl
Fahr’s syndrome and clinical correlation: a case series and literature review Page 1 282 Folia
Neuropathologica 2016; 54/3 Case report Fahr’s syndrome and clinical correlation: a case series …
Neuropathologica 2016; 54/3 Case report Fahr’s syndrome and clinical correlation: a case series …
[HTML][HTML] Neuropsychiatric manifestations of fahr's disease, diagnostic and therapeutic challenge: A case report and a literature review
MG Carbone, F Della Rocca - Clinical Neuropsychiatry, 2022 - ncbi.nlm.nih.gov
Objective Calcifications in basal ganglia could be an incidental finding up to 20% of
asymptomatic patients undergoing computed tomography (CT) or magnetic resonance …
asymptomatic patients undergoing computed tomography (CT) or magnetic resonance …
A case of psychosis due to Fahr's syndrome and response to behavioral disturbances with risperidone and oxcarbazepine
AD Faye, S Gawande, R Tadke… - Indian journal of …, 2014 - journals.lww.com
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 …
and symmetrical intracranial deposition of calcium mainly in cerebral basal ganglia. Motor …
Idiopathic young-onset Fahr's disease with schizophrenia-like presentation: a case report
WC Li, YC Hsieh, PT Chen, CN Lee, TY Tsai - Frontiers in Psychiatry, 2024 - frontiersin.org
This case report describes an exceptionally rare case in which a prior diagnosis of
schizophrenia was later determined to be early-onset Fahr's disease, linked to a genetic …
schizophrenia was later determined to be early-onset Fahr's disease, linked to a genetic …
A novel homozygous 10 nucleotide deletion in BBS10 causes Bardet–Biedl syndrome in a Pakistani family
Bardet–Biedl Syndrome is a multisystem autosomal recessive disorder characterized by
central obesity, polydactyly, hypogonadism, learning difficulties, rod-cone dystrophy and …
central obesity, polydactyly, hypogonadism, learning difficulties, rod-cone dystrophy and …
[PDF][PDF] Fahr's disease: a rare neurological disease frequently misdiagnosed as acute psychosis, or mood disorder
Fahr's disease is a rare, degenerative neurological disorder characterized by idiopathic
symmetrical and bilateral intracranial calcification. We present a case of 32 years old man …
symmetrical and bilateral intracranial calcification. We present a case of 32 years old man …
Fahr's syndrome due to hypoparathyroidism following thyroidectomy
FB Soares, FF Amorim, AR Santana… - Journal of Medical …, 2013 - journalmc.org
Fahr's syndrome is a rare, degenerative, and neuropsychiatric disorder characterized by
seizures, extrapyramidal and neuropsychiatric symptoms as a result of symmetric and …
seizures, extrapyramidal and neuropsychiatric symptoms as a result of symmetric and …
Psychosis associated with Fahr's syndrome: a case report
CA Cassiani-Miranda, M Herazo-Bustos… - Revista Colombiana …, 2015 - scielo.org.co
Abstract CASSIANI-MIRANDA, Carlos Arturo et al. Psychosis Associated With Fahr's
Syndrome: A Case Report. rev. colomb. psiquiatr.[online]. 2015, vol. 44, n. 4, pp. 256-261 …
Syndrome: A Case Report. rev. colomb. psiquiatr.[online]. 2015, vol. 44, n. 4, pp. 256-261 …
FAHR'S Sy ndrome: A rare Neurodegenerative Disorder
Abstract Idiopathic Basal Ganglia Calcification, also known as Fahr disease or Fahr's
Syndrome or Bilateral StriatoPallidoDentate Calcinosis (BSPDC) is a rare, genetically …
Syndrome or Bilateral StriatoPallidoDentate Calcinosis (BSPDC) is a rare, genetically …