Bowirrat Abdalla, Yassin Mustafa, Artoul Faozi, Artul Suheil
Department of Neuroscience, EMMS Nazareth Hospital, Nazareth, Israel.
BMJ Case Rep. 2013 Sep 6;2013:bcr2013200462. doi: 10.1136/bcr-2013-200462.
Bilateral striopallidodentate calcinosis, commonly known as Fahr's disease is a rare clinical entity present mainly with extrapyramidal signs and accompanied with metabolic, biochemical, neuroradiological and neuropsychiatric situations. It is characterised by the symmetrical and bilateral intracranial deposition of calcium associated with cell loss in the basal ganglia, cerebral cortex and cerebellum.In this study, we discussed two brothers' cases of Fahr's diseases who presented with different symptomatology. The first presented with walking difficulty, cramps and dysarthria and moderate memory impairment whereas the second with vertigo, ataxia, forgetfulness and headache. CT scans of both patients revealed intracranial diffuse bilateral calcifications in the basal ganglia and the cerebellum. The second patient revealed progressive cerebral atrophy but reduction in the calcification. Fahr's disease, although encountered rarely, should also be taken into account in the differential diagnosis of cases with abnormal intracranial calcifications along with other familial, congenital and metabolic diseases and syndromes.
双侧纹状体苍白球齿状核钙化,通常称为法尔病,是一种罕见的临床病症,主要表现为锥体外系症状,并伴有代谢、生化、神经放射学和神经精神方面的情况。其特征是双侧对称性颅内钙沉积,并伴有基底神经节、大脑皮层和小脑的细胞丢失。在本研究中,我们讨论了两兄弟患法尔病的病例,他们表现出不同的症状。第一个表现为行走困难、痉挛和构音障碍以及中度记忆障碍,而第二个表现为眩晕、共济失调、健忘和头痛。两名患者的CT扫描均显示基底神经节和小脑存在颅内弥漫性双侧钙化。第二名患者显示出进行性脑萎缩,但钙化有所减少。法尔病虽然很少见,但在颅内钙化异常病例的鉴别诊断中,也应与其他家族性、先天性和代谢性疾病及综合征一并考虑。