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胱氨酸病性脑病的临床多态性。半胱胺治疗结果

Clinical polymorphism of cystinosis encephalopathy. Results of treatment with cysteamine.

作者信息

Broyer M, Tête M J, Guest G, Berthélémé J P, Labrousse F, Poisson M

机构信息

Department of Pediatric Nephrology, Hôpital Necker-Enfants Malades, Paris, France.

出版信息

J Inherit Metab Dis. 1996;19(1):65-75. doi: 10.1007/BF01799350.

Abstract

Of the 26 cystinotic patients over 19 years of age followed in our institution, 7 developed CNS complications at a mean age of 23 years. Two forms were observed. The first, associating cerebellar and pyramidal signs, mental deterioration and finally pseudo-bulbar palsy, may be called cystinosis encephalopathy. The other form resembled a stroke-like episode with coma and hemiplegia or milder symptoms. Hydrocephalus was rare and not associated with clinical symptoms in this series. Cysteamine was administered for longer than 6 months to 4 of the patients with encephalopathy. Two had an almost complete disappearance of their symptoms including the gross abnormalities of MR imaging in one; one improved partially and remained stable, and one continued to deteriorate but was suspected of non-compliance. These results suggest that cysteamine may be an effective treatment of cystinosis encephalopathy and encourage prescription of this drug in cystinosis in order to prevent this complication.

摘要

在我们机构随访的26例19岁以上的胱氨酸病患者中,7例在平均23岁时出现中枢神经系统并发症。观察到两种形式。第一种,伴有小脑和锥体束征、智力衰退,最终出现假性延髓麻痹,可称为胱氨酸病脑病。另一种形式类似于中风样发作,伴有昏迷和偏瘫或症状较轻。在本系列中,脑积水罕见且与临床症状无关。4例脑病患者接受半胱胺治疗超过6个月。其中2例症状几乎完全消失,包括1例磁共振成像的明显异常;1例部分改善并保持稳定,1例继续恶化,但怀疑未遵医嘱。这些结果表明,半胱胺可能是治疗胱氨酸病脑病的有效方法,并鼓励在胱氨酸病中使用这种药物以预防这种并发症。

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