新生儿发育迟缓症:它仍然是诊断难题吗?系统综述提供的证据。

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Journal of Child Neurology Pub Date : 2024-10-01 Epub Date: 2024-09-02 DOI:10.1177/08830738241273425
Raffaele Falsaperla, Vincenzo Sortino, Valentina Giacchi, Marco Andrea Nicola Saporito, Silvia Marino, Lucia Giovanna Tardino, Lidia Marino, Alessia Gennaro, Martino Ruggieri, Chiara Barberi, Agata Polizzi
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引用次数: 0

摘要

过度惊跳症是一种神经系统疾病,其特征是对不同类型的刺激产生夸张的惊跳反射。过度惊跳症的定义是新生儿张力过高、过度惊跳反射和惊跳后全身僵硬三联征。本研究的目的是找出已确诊为遗传性新生儿惊跳过度症的病例,并确定发病时基因型与表型之间的相关性。研究选取了 1993 年至 2024 年间的文章,并应用了 PRISMA 声明,其中包括出生 28 天内的新生儿。因此,我们从文献中检索到了 14 例经基因确诊的新生儿高热惊厥病例。14 例患者中有 8 例(57.14%)的临床表现在出生后第一天出现。临床表现为肌肉僵硬(100%)、惊跳反射(66.66%)、呼吸暂停/青紫(41.66%)、拍鼻试验阳性(33.33%)、抽搐(33.33%)、抖动(25%)和发作性眨眼(25%)。14 人中有 9 人(64.28%)涉及 GLRA1 基因,14 人中有 2 人(14.28%)涉及 SLC6A5 基因,14 人中有 1 人(7.14%)涉及 GPHN 基因,14 人中有 2 人(14.28%)涉及 GLRB 基因。患者表现为杂合(66.66%)或同源(33.33%)状态。在 14 例患者中,有 7 例(50%)的其他家庭成员也患有此病。及时诊断对改善过度惊厥的自然病史至关重要,可避免/减少可能出现的重大并发症,如婴儿猝死综合征、脑损伤和严重跌倒。及早与癫痫相鉴别可最大限度地降低治疗成本,提高患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neonatal Hyperekplexia: Is It Still a Diagnostic Challenge? Evidence From a Systematic Review.

Hyperekplexia is a neurologic disorder characterized by an exaggerated startle reflex in response to different types of stimuli. Hyperekplexia is defined by the triad of neonatal hypertonia, excessive startle reflexes, and generalized stiffness following the startle. Although uncommon, hyperekplexia can lead to serious consequences such as falls, brain injury, or sudden infant death syndrome.Aim of this study was to identify cases of neonatal hyperekplexia with a confirmed genetic diagnosis and to establish the genotype-phenotype correlation at onset. Articles were selected from 1993 to 2024 and PRISMA Statement was applied including newborns within 28 days of life. So, we retrieved from literature 14 cases of genetically confirmed neonatal hyperekplexia. The onset of clinical manifestations occurred in the first day of life in 8 of 14 patients (57.14%). Clinical findings were muscle stiffness (100%), startle reflex (66.66%), apnea/cyanosis (41.66%), positive nose-tapping test (33.33%), jerks (33.33%), jitteriness (25%), and ictal blinking (25%). Genes involved were GLRA1 in 9 of 14 (64.28%), SLC6A5 in 2 of 14 (14.28%), GPHN in 1 of 14 (7.14%), and GLRB in 2 of 14 (14.28%). Patients showed heterozygous (66.66%) or homozygous (33.33%) status. In 7 of 14 cases (50%), the condition occurred in other family members. A genotype-phenotype correlation was not achievable.Timely diagnosis is crucial to improve the natural history of hyperekplexia avoiding/reducing possible major complications such as sudden infant death syndrome, brain injury, and serious falls. Early differentiation from epilepsy minimizes treatment cost and improves the quality of life of patients.

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来源期刊
Journal of Child Neurology
Journal of Child Neurology 医学-临床神经学
CiteScore
4.20
自引率
5.30%
发文量
111
审稿时长
3-6 weeks
期刊介绍: The Journal of Child Neurology (JCN) embraces peer-reviewed clinical and investigative studies from a wide-variety of neuroscience disciplines. Focusing on the needs of neurologic patients from birth to age 18 years, JCN covers topics ranging from assessment of new and changing therapies and procedures; diagnosis, evaluation, and management of neurologic, neuropsychiatric, and neurodevelopmental disorders; and pathophysiology of central nervous system diseases.
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