Jul 19, 2024 · What is Fahr's syndrome? Fahr's syndrome is a rare, genetically dominant, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement, including the basal ganglia and the cerebral cortex.

Aug 13, 2023 · Fahr disease is a rare neurological condition characterized by abnormal idiopathic calcification of basal ganglia and commonly has an autosomal dominant inheritance. This activity describes the pathophysiology, etiology, differential diagnosis, evaluation, and treatment of Fahr disease and highlights the role of the interprofessional team in ...

Jan 8, 2024 · Fahr’s syndrome refers to a rare brain disorder that can occur when a person inherits certain gene alterations. Atypical amounts of calcium can gather in the parts of the brain responsible...

原发性甲状旁腺功能减退造成的Fahr综合征，病程长有多次发作性手足抽搐史，有舞蹈、手足徐动或 帕金森病 样表现小脑性 共济失调 或少数患者有双侧肢体锥体束征阳性。

两侧对称性大脑 基底核钙化可以由许多原因造成，故这种表现实际是一种综合征，称之为两侧对称性大脑 基底核钙化 综合征，又称Fahr综合征（Fahrs’s syndrome）。

Jan 16, 2025 · Fahr病（Fahr’s disease，FD），也称为家族性特发性基底神经节钙化或双侧苍白球齿状突钙化症，是一种罕见的以丘脑、基底神经节、大脑皮质和小脑齿状核内异常血管钙沉积为特征的疾病。

Jul 1, 2023 · Fahr病是一种罕见的神经退行性疾病，由Theodor Fahr于1930年首次描述，其定义为基底神经节和大脑皮质中的异常钙化沉积。Fahr病通常影响年轻至中年成人，具有各种临床表现，包括内分泌、皮肤和神经问题，锥体外系症状是最常见的表现。

Fahr's Syndrome, also known as Primary Familial Brain Calcification (PFBC), is a rare neurological disorder characterized by bilateral calcification of the basal ganglia and other brain regions. First documented by German neurologist Karl Theodor Fahr in 1930, this condition affects approximately 1 in 1,000,000 individuals.

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 made up of calcium carbonate and calcium phosphate, and are commonly located in the Basal Ganglia, Thalamus, Hippocampus, Cerebral cortex, Cerebellar Subcortical white ...

Aug 13, 2023 · Fahr disease is named after Karl Theodor Fahr, a German neurologist who first reported the disorder in 1930. It is a rare neurological condition characterized by abnormal idiopathic calcification of basal ganglia and commonly has an autosomal dominant inheritance.