Larbrisseau A, Carpenter S
Neuropediatrics. 1982 May;13(2):95-8. doi: 10.1055/s-2008-1059605.
Rud syndrome consists in the association of oligophrenia and hypogonadism with congenital ichthyosis; in the majority of cases, epilepsy, short stature or delayed in growth are also found. We described a child with such a syndrome. In addition to the classical findings, the patient had retinitis pigmentosa and hypertrophic polyneuropathy. Histological studies, including ultrastructural findings of a sural nerve biopsy, showed signs of a chronic demyelinative neuropathy with onion bulb formation. The world literature was reviewed and only nine other cases fulfilled our criteria for inclusion in Rud syndrome. This case represents the one with the most extensive neurological involvement ever reported.
鲁德综合征表现为智力发育迟缓、性腺功能减退与先天性鱼鳞病并存;大多数情况下,还会出现癫痫、身材矮小或生长发育迟缓。我们描述了一名患有该综合征的儿童。除了典型表现外,该患者还患有色素性视网膜炎和肥厚性多发性神经病。组织学研究,包括腓肠神经活检的超微结构结果,显示出慢性脱髓鞘性神经病伴洋葱球形成的迹象。我们查阅了世界文献,仅有其他9例符合我们纳入鲁德综合征的标准。该病例是有史以来报道的神经受累最广泛的病例。