Cyclic Vomiting Syndrome in Patients Affected by Jansen-de Vries Syndrome: Results From an International Survey.

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
A Pizzol, K A Adams, B B A de Vries, C J Curry, P L Calvo
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Abstract

Jansen-de Vries syndrome (JdVS) is an autosomal dominant neurodevelopmental disorder with intellectual disability and gastrointestinal (GI) abnormalities, including recurrent vomiting. This study aimed to understand the frequency and severity of GI symptoms in JdVS patients and to investigate the potential association with cyclic vomiting syndrome (CVS), which has not been previously reported. An international online survey assessed the prevalence and features of CVS and GI disorders in JdVS patients using Rome IV Criteria. The anonymous survey was conducted via Google Forms in April 2021. A total of 21 patients/guardians responded to the survey. The average age at JdVS diagnosis was 8.22 years (range: 1-42). Of the respondents, 6 (28.5%) had a CVS diagnosis, 5 (23.8%) had migraine, and 2 (9.5%) had abdominal migraine. Additionally, 8 (38%) had gastroesophageal reflux disease (GERD) and 8 (38%) had functional constipation. An analysis targeted questions showed that 7 (33%) met the Rome IV Criteria for CVS but were undiagnosed, leading to a CVS prevalence of 61% in this cohort. This study highlights a high prevalence of CVS in JdVS patients and underscores the need for increased awareness and accurate diagnosis to address misdiagnosis.

扬森-德-弗里斯综合征患者的周期性呕吐综合征:一项国际调查的结果。
詹森-德-弗里斯综合征(JdVS)是一种常染色体显性遗传的神经发育障碍性疾病,伴有智力障碍和胃肠道(GI)异常,包括反复呕吐。本研究旨在了解 JdVS 患者胃肠道症状的发生频率和严重程度,并调查其与周期性呕吐综合征(CVS)之间的潜在关联,此前尚未有相关报道。一项国际在线调查采用罗马IV标准评估了JdVS患者中CVS和消化道疾病的患病率和特征。匿名调查于 2021 年 4 月通过谷歌表格进行。共有 21 名患者/监护人回复了调查。确诊 JdVS 时的平均年龄为 8.22 岁(范围:1-42 岁)。受访者中,6 人(28.5%)确诊为 CVS,5 人(23.8%)患有偏头痛,2 人(9.5%)患有腹型偏头痛。此外,8 人(38%)患有胃食管反流病(GERD),8 人(38%)患有功能性便秘。针对问题的分析表明,有 7 人(33%)符合 CVS 的罗马 IV 标准,但未得到诊断,因此该队列中的 CVS 患病率为 61%。这项研究强调了 JdVS 患者中 CVS 的高患病率,并强调了提高意识和准确诊断以解决误诊问题的必要性。
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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