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甘露糖苷贮积症的临床病程。

The clinical course of mannosidosis.

作者信息

Autio S, Louhimo T, Helenius M

出版信息

Ann Clin Res. 1982 Apr;14(2):93-7.

PMID:7149616
Abstract

The clinical course of mannosidosis was studied in eight patients. The age at onset of symptoms varied from 6 months to 3 years. The first symptom was usually delayed development of speech or motor or mental functions and was often accompanied by recurrent infections. All the patients were mentally retarded, with slightly coarse facial features, poor ability to speak, sensorineural hearing loss and dysostosis multiplex. Ataxia was seen in all but one case, appearing in childhood at the same time as the hearing loss. Follow-up observations suggested gradual impairment of mental and motor functions and speech with age. Other findings were stunted growth in adults, and vacuolated lymphocytes in the peripheral blood.

摘要

对8例甘露糖苷贮积症患者的临床病程进行了研究。症状出现的年龄从6个月至3岁不等。首发症状通常是言语、运动或智力功能发育迟缓,常伴有反复感染。所有患者均有智力障碍,面部特征略显粗糙,语言能力差,感音神经性听力损失和多发性骨发育异常。除1例患者外,其余患者均有共济失调,在儿童期与听力损失同时出现。随访观察表明,随着年龄增长,智力、运动功能和语言逐渐受损。其他发现包括成人生长发育迟缓以及外周血中出现空泡化淋巴细胞。

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