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[一例青少年急性可逆性自主神经功能障碍病例]

[A case of acute reversible dysautonomia in an adolescent].

作者信息

Bost M, Rossignol A M, Tachker D, Batellier H, Jeannoel P

出版信息

Pediatrie. 1983 Jan-Feb;38(1):29-36.

PMID:6866640
Abstract

A 16 years old male presented with orthostatic hypotension with constant pulse, associated with severe constipation, decrease of sudoral secretions, weight loss and asthenia. This dysautonomia evolued during a period of 6 months and disappeared completely leaving no sequellaes. The symptoms appeared after a rubella. The authors discuss the originality of this observation among the pure pan-dysautonomia and the modes of exploration of the autonomic nervous system. Its mechanisms is probably auto-immune.

摘要

一名16岁男性出现体位性低血压伴脉搏恒定,伴有严重便秘、汗液分泌减少、体重减轻和乏力。这种自主神经功能障碍在6个月内逐渐发展,随后完全消失,未留下后遗症。症状出现在风疹之后。作者讨论了这一病例在单纯性全自主神经功能障碍中的独特性以及自主神经系统的检查方式。其机制可能是自身免疫性的。

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