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家族性自主神经功能异常中的味觉和嗅觉

Taste and smell in familial dysautonomia.

作者信息

Gadoth N, Mass E, Gordon C R, Steiner J E

机构信息

Department of Neurology, Rabin Medical Center, Petah Tiqva, Israel.

出版信息

Dev Med Child Neurol. 1997 Jun;39(6):393-7.

PMID:9233364
Abstract

Familial dysautonomia (FD) is one of the classic diseases characterised by taste and smell abnormalities. However, these typical features are based on data obtained from two separate crude studies published in 1964. In the present study psychophysical-cognitive and reflex-like facial-behavioral responses to taste and smell, in nine patients with FD and 15 healthy controls, were recorded. Five taste stimulants were presented to both study groups, while a selection of common household odors was used for FD patients only. The patients with FD showed a markedly higher incidence of recognition failures for salty, bitter, sweet, and water stimuli than the controls, but rate of recognition of sour stimuli was almost identical in the two groups. Estimates by the subjects on a hedonic scale of 0 to 10 and facial display in FD indicated a relatively normal sensitivity to sour stimuli and to a lesser extent to bitter stimuli. Water, sweet, and salty stimuli evoked non-discriminatory responses. These findings indicate specific dyageusia rather than general ageusia. Smell was found to be normal. In children with taste and smell impairment, a systematic evaluative approach may help in planning palatable diets for adequate and comfortable nutrition.

摘要

家族性自主神经功能障碍(FD)是一种以味觉和嗅觉异常为特征的经典疾病。然而,这些典型特征是基于1964年发表的两项单独的粗略研究获得的数据。在本研究中,记录了9名FD患者和15名健康对照者对味觉和嗅觉的心理物理认知及类似反射的面部行为反应。向两个研究组呈现了五种味觉刺激物,而仅对FD患者使用了一系列常见的家庭气味。FD患者对咸、苦、甜和水刺激的识别失败发生率明显高于对照组,但两组对酸刺激的识别率几乎相同。FD患者在0至10的享乐量表上的估计以及面部表现表明,他们对酸刺激的敏感性相对正常,对苦刺激的敏感性较低。水、甜和咸刺激引发了非辨别性反应。这些发现表明是特定的味觉障碍而非一般性味觉丧失。嗅觉被发现是正常的。对于有味觉和嗅觉障碍的儿童,一种系统的评估方法可能有助于规划可口的饮食,以实现充足且舒适的营养。

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