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婴儿期良性阵发性斜颈:4例新病例及与CACNA1A突变的关联

Benign paroxysmal torticollis of infancy: four new cases and linkage to CACNA1A mutation.

作者信息

Giffin N J, Benton S, Goadsby P J

机构信息

Headache Group, Institute of Neurology, London, UK.

出版信息

Dev Med Child Neurol. 2002 Jul;44(7):490-3. doi: 10.1017/s0012162201002407.

Abstract

Benign paroxysmal torticollis of infancy (BPTI) is a disorder characterized by recurrent episodes of head tilt secondary to cervical dystonia. Attacks are often accompanied by vomiting, pallor, and ataxia, settling spontaneously within hours or days. Episodes begin within the first 12 months of life and resolve by 5 years. We report four patients with BPTI. Symptoms started from 3 months of age, with head tilting lasting between 10 minutes and 2 months; the shorter episodes were followed by vomiting, apathy, and unsteadiness. Head tilt became less prominent after infancy, replaced by vertigo and eventually by migraine headaches. Two patients came from a kindred with familial hemiplegic migraine linked to CACNA1A mutation. BPTI may be regarded as a migraine aura equivalent. The syndrome poses interesting questions regarding varying phenotypic expression of calcium channelopathies at different stages of development.

摘要

婴儿良性阵发性斜颈(BPTI)是一种以继发于颈部肌张力障碍的反复性头部倾斜发作为特征的疾病。发作常伴有呕吐、面色苍白和共济失调,数小时或数天内可自行缓解。发作始于出生后的头12个月内,5岁时缓解。我们报告了4例BPTI患者。症状始于3个月大,头部倾斜持续10分钟至2个月;较短的发作后伴有呕吐、冷漠和不稳。婴儿期后头部倾斜变得不那么明显,被眩晕取代,最终被偏头痛取代。2例患者来自一个与CACNA1A突变相关的家族性偏瘫性偏头痛家族。BPTI可被视为偏头痛等位发作。该综合征在发育的不同阶段就钙通道病不同的表型表达提出了有趣的问题。

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