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新生儿期中央核性肌病导致严重呼吸窘迫。

Centronuclear myopathy in the newborn period causing severe respiratory distress.

作者信息

Raju T N, Vidyasagar D, Reyes M G, Chokroverty S

出版信息

Pediatrics. 1977 Jan;59(1):29-34.

PMID:840536
Abstract

Centronuclear myopathy can be classified into four clinical varieties based on age, severity at onset, and rapidity of progress. In the severe form with involvement of respiratory muscles at birth, the progress is rapid and fatal before 3 years of age. The case described in this report illustrates rapid progression of muscle paralysis and death in a neonate. However, in a majority of cases the disease is either moderately severe or mild with the affected individuals confined to wheel chair by adolescence or early adult life. Diagnosis of the disease is based on appropriate muscle histopathology and electron microscopic studies.

摘要

中央核性肌病可根据发病年龄、起病时的严重程度以及进展速度分为四种临床类型。在出生时即累及呼吸肌的严重类型中,病情进展迅速,在3岁前死亡。本报告中描述的病例显示了一名新生儿肌肉麻痹的快速进展和死亡。然而,在大多数病例中,疾病为中度严重或轻度,受影响个体在青春期或成年早期需依靠轮椅行动。该病的诊断基于适当的肌肉组织病理学和电子显微镜研究。

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