Callender J S
Royal Cornhill Hospital, Aberdeen, UK.
J Neurol Neurosurg Psychiatry. 1995 Oct;59(4):432-4. doi: 10.1136/jnnp.59.4.432.
The clinical features and long term outcome of familial idiopathic intracranial calcification in three members of one family are described. The illness presented as psychiatric disorder in all patients, and in one patient, epilepsy and intellectual deterioration were later manifestations. Skull radiographs and CT were performed sequentially, in one patient, over a 22 year period and, in another, CT was carried out eight years apart. In neither patient was there any evidence of progression of calcification.
本文描述了一个家族中三名成员的家族性特发性颅内钙化的临床特征和长期预后。所有患者均以精神障碍为首发表现,其中一名患者后来出现癫痫和智力衰退。在一名患者中,颅骨X光片和CT在22年期间相继进行,另一名患者的CT检查间隔8年。两名患者均未发现钙化进展的证据。