Cerebral gigantism associated with jaw cyst basal cell naevoid syndrome in two families.

H Cramer, H Niederdellmann
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引用次数: 5

Abstract

We report 9 subjects from 2 families with the syndrome of cerebral gigantism, seven of the patients also had jaw cyst basal cell naevoid syndrome. Neurological, radiological, somatic and biochemical features of this hitherto unreported association are described. Neurological symptoms included mild hydrocephalus, ventricular malformation, cerebellar syndrome, intracranial calcification, oculomotor disturbances, EEG abnormalities and rarely, mild peripheral nervous disorders. A disturbance of calcium metabolism appears to be a prominent feature of the genetically determined nonprogressive syndrome.

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脑巨人症与两家系颌骨囊肿基底细胞痣样综合征相关。
我们报告了来自2个家族的9例脑巨人症患者,其中7例同时伴有颌骨囊肿基底细胞痣样综合征。神经学,放射学,体细胞和生化特征,这种迄今未报道的关联描述。神经系统症状包括轻度脑积水、脑室畸形、小脑综合征、颅内钙化、动眼力障碍、脑电图异常和罕见的轻度周围神经障碍。钙代谢紊乱似乎是基因决定的非进行性综合征的一个突出特征。
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