[PDF][PDF] Fahr's syndrome: diagnosis issues in patients with unknown family history of disease
Fahr's disease (FD) is a rare clinical neurodegenerative entity, occurring in fourth or fifth
decade or elderly patients, consisting in symmetric polytopic calcifications, in one ore more …
decade or elderly patients, consisting in symmetric polytopic calcifications, in one ore more …
[HTML][HTML] Fahr syndrome–an important piece of a puzzle in the differential diagnosis of many diseases
K Jaworski, M Styczyńska, M Mandecka… - Polish journal of …, 2017 - ncbi.nlm.nih.gov
Fahr syndrome is a rare neurodegenerative disorder characterized by symmetrical, bilateral
calcifications in the basal ganglia, nucleus gyrus and cerebral cortex. The continuous …
calcifications in the basal ganglia, nucleus gyrus and cerebral cortex. The continuous …
[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: two case report
N Khammassi, J Chrifi, D Mohsen… - Revue …, 2010 - pubmed.ncbi.nlm.nih.gov
Introduction Fahr's syndrome is characterized by symmetrical and bilateral intracerebral
calcifications, located in the basal ganglia and mostly associated with a phosphorus calcium …
calcifications, located in the basal ganglia and mostly associated with a phosphorus calcium …
[HTML][HTML] Fahr's syndrome: literature review of current evidence
S Saleem, HM Aslam, M Anwar, S Anwar… - Orphanet journal of rare …, 2013 - Springer
Fahr's disease or Fahr's syndrome is a rare, neurological disorder characterized by
abnormal calcified deposits in basal ganglia and cerebral cortex. Calcified deposits are …
abnormal calcified deposits in basal ganglia and cerebral cortex. Calcified deposits are …
[PDF][PDF] Fahr's disease: An incidental finding in a case presenting with psychosis
S Srivastava, MS Bhatia, V Sharma, S Mahajan… - Ger J …, 2010 - researchgate.net
Fahr's syndrome refers to a rare syndrome characterized by symmetrical and bilateral
intracranial calcification. We present a 24-year-old male with Fahr disease, presenting with …
intracranial calcification. We present a 24-year-old male with Fahr disease, presenting with …
Familial Fahr disease in a Turkish family.
Fahr syndrome refers to a rare syndrome characterized by symmetrical and bilateral
intracranial calcification. We present a 42-year-old woman with Fahr disease, but lacking …
intracranial calcification. We present a 42-year-old woman with Fahr disease, but lacking …
[HTML][HTML] Advanced Early-Onset Fahr's Disease: A Case Report
K Aghemo, R Salmanzadeh, O DeAngelo… - Cureus, 2023 - ncbi.nlm.nih.gov
Fahr's disease is a rare disorder characterized by abnormal calcium deposition within the
basal ganglia, cerebellar dentate nuclei, and white matter tracts with subsequent atrophy …
basal ganglia, cerebellar dentate nuclei, and white matter tracts with subsequent atrophy …
[HTML][HTML] Fahr's syndrome presenting as pre-senile dementia with Behavioral abnormalities: a rare case report
AS Ghogare, S Nemade - Cureus, 2021 - ncbi.nlm.nih.gov
Fahr's syndrome is a rare neurological disorder characterized by bilateral basal ganglia
calcification. Calcification may also involve other brain areas like dentate nuclei of the …
calcification. Calcification may also involve other brain areas like dentate nuclei of the …
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 …