• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

先天性甲状腺功能减退症及相关的视动和智力发育

Congenital hypothyroidism and associated visual-motor and intellectual development.

作者信息

Ontiveros-Mendoza Esperanza, González-Medrano Juan Antonio, Rivera-González Rolando, Sánchez-Huerta Karla, Sánchez Carmen, Barragán-Mejía Gerardo

机构信息

Centro de Investigación en Neurodesarrollo. Instituto Nacional de Pediatría, Mexico City, México.

Universidad Autónoma Metropolitana-Unidad Xochimilco, Mexico City, México.

出版信息

Pediatr Res. 2025 Jan 22. doi: 10.1038/s41390-025-03850-3.

DOI:10.1038/s41390-025-03850-3
PMID:39843775
Abstract

BACKGROUND

Congenital hypothyroidism's sequelae include visuomotor and intellectual developmental deficits. Visual-motor perception is a cognitive function related to academic performance. Intellect is the ability to learn and use acquired knowledge to solve and achieve goals. Our objective was to evaluate visual-motor and intellectual development in children with late initiation of treatment for congenital hypothyroidism enrolled in a developmental follow-up and intervention program.

METHODS

We evaluated the visual-motor and intellectual development of 75 infants with congenital hypothyroidism, 34 with athyrosis, and 41 with ectopia using the Bender Visual-Motor Development Test and the Weschler Intelligence Scale at eight and nine years of age.

RESULTS

Children with ectopia had a visual-motor delay of -2 years and an Intelligence Quotient (IQ) greater than 98 points. Children with athyrosis had a visual-motor delay equivalent to -3.2 years and an IQ below 90 points. Better performance on Bender's test was positively correlated with IQ. Attending more than 80% of Developmental Intervention Program appointments had a positive impact on intellectual development.

CONCLUSIONS

Timely diagnosis and early treatment with the appropriate dose of levothyroxine are determining factors; however, attendance to a development follow-up and intervention program could further support the cognitive development of children with congenital hypothyroidism.

IMPACT

Visuomotor development influences cognitive functions related to school performance. Deficits in the ability to learn and use acquired knowledge to solve problems and achieve goals are characteristic of children with congenital hypothyroidism. Delayed treatment is associated with more severe sequelae in both visual-motor and intellectual development. Here, we show that treatment with adequate doses of levothyroxine and inclusion in a follow-up and developmental program are highly recommended for patients with delayed treatment. A better understanding of these factors will allow clinicians to target therapeutic interventions.

摘要

背景

先天性甲状腺功能减退症的后遗症包括视觉运动和智力发育缺陷。视觉运动感知是一种与学业成绩相关的认知功能。智力是学习和运用所学知识解决问题并实现目标的能力。我们的目的是评估参加发育随访和干预项目的先天性甲状腺功能减退症治疗起步较晚的儿童的视觉运动和智力发育情况。

方法

我们使用本德尔视觉运动发育测试和韦氏智力量表,在8岁和9岁时评估了75例先天性甲状腺功能减退症婴儿、34例甲状腺缺如婴儿和41例异位甲状腺婴儿的视觉运动和智力发育情况。

结果

异位甲状腺患儿的视觉运动延迟达2年,智商高于98分。甲状腺缺如患儿的视觉运动延迟相当于3.2年,智商低于90分。本德尔测试表现较好与智商呈正相关。参加超过80%的发育干预项目预约对智力发育有积极影响。

结论

及时诊断并使用适当剂量的左甲状腺素进行早期治疗是决定性因素;然而,参加发育随访和干预项目可以进一步支持先天性甲状腺功能减退症患儿的认知发育。

影响

视觉运动发育影响与学业成绩相关的认知功能。学习和运用所学知识解决问题并实现目标的能力缺陷是先天性甲状腺功能减退症患儿的特征。治疗延迟与视觉运动和智力发育方面更严重的后遗症相关。在此,我们表明,对于治疗延迟的患者,强烈建议使用适当剂量的左甲状腺素进行治疗并纳入随访和发育项目。更好地理解这些因素将使临床医生能够针对性地进行治疗干预。

相似文献

1
Congenital hypothyroidism and associated visual-motor and intellectual development.先天性甲状腺功能减退症及相关的视动和智力发育
Pediatr Res. 2025 Jan 22. doi: 10.1038/s41390-025-03850-3.
2
[Cognitive performance of preschoolers with Congenital Hypothyroidism enrolled in a follow-up program].[参加随访项目的先天性甲状腺功能减退症学龄前儿童的认知表现]
Andes Pediatr. 2023 Jan;94(1):62-69. doi: 10.32641/andespediatr.v94i1.4356.
3
Intellectual and motor development of young adults with congenital hypothyroidism diagnosed by neonatal screening.通过新生儿筛查诊断出的先天性甲状腺功能减退症青年的智力和运动发育
J Clin Endocrinol Metab. 2006 Feb;91(2):418-24. doi: 10.1210/jc.2005-1209. Epub 2005 Nov 22.
4
Neurodevelopmental and body composition outcomes in children with congenital hypothyroidism treated with high-dose initial replacement and close monitoring.先天性甲状腺功能减退症患儿采用高剂量初始替代治疗和密切监测的神经发育和身体成分结果。
J Clin Endocrinol Metab. 2013 Sep;98(9):3663-70. doi: 10.1210/jc.2013-1903. Epub 2013 Jul 16.
5
Effect of different starting doses of levothyroxine on growth and intellectual outcome at four years of age in congenital hypothyroidism.先天性甲状腺功能减退症中不同起始剂量左甲状腺素对4岁时生长发育和智力发育的影响。
Thyroid. 2002 Jan;12(1):45-52. doi: 10.1089/105072502753451968.
6
Intellectual outcome of patients with congenital hypothyroidism detected by neonatal screening.通过新生儿筛查发现的先天性甲状腺功能减退症患者的智力发育结果。
J Formos Med Assoc. 2001 Jan;100(1):40-4.
7
Intellectual outcome at 12 years of age in congenital hypothyroidism.先天性甲状腺功能减退症患儿12岁时的智力发育结果。
Eur J Endocrinol. 1999 Aug;141(2):105-10. doi: 10.1530/eje.0.1410105.
8
Intellectual development in preschool children with early treated congenital hypothyroidism.早期接受治疗的先天性甲状腺功能减退症学龄前儿童的智力发育
Ann Pediatr Endocrinol Metab. 2017 Jun;22(2):102-107. doi: 10.6065/apem.2017.22.2.102. Epub 2017 Jun 28.
9
Late Diagnosis of Congenital Hypothyroidism in Young Adult.青年成人先天性甲状腺功能减退症的延迟诊断
Acta Med Indones. 2019 Jul;51(3):272-274.
10
Intellectual outcomes of patients with congenital hypothyroidism not detected by neonatal screening.新生儿筛查未检出的先天性甲状腺功能减退症患者的智力发育结果
J Formos Med Assoc. 1999 Jul;98(7):512-5.

本文引用的文献

1
Neuropsychological Alterations in Patients with Congenital Hypothyroidism Treated with Levothyroxine: Linked Factors and Thyroid Hormone Hyposensitivity.左甲状腺素治疗的先天性甲状腺功能减退症患者的神经心理学改变:相关因素与甲状腺激素低敏性
J Clin Med. 2022 Jun 15;11(12):3427. doi: 10.3390/jcm11123427.
2
Levothyroxine treatment for congenital hypothyroidism based on thyroid function: a 10-year clinical retrospective study.基于甲状腺功能的左旋甲状腺素治疗先天性甲状腺功能减退症:一项 10 年临床回顾性研究。
BMC Endocr Disord. 2022 May 28;22(1):142. doi: 10.1186/s12902-022-01061-z.
3
[Formula: see text]Socioeconomic aspects are crucial to better intellectual outcome in early-treated adolescents with congenital hypothyroidism.
[公式:见正文]社会经济方面对于先天性甲状腺功能减退症的早期治疗青少年的智力预后改善至关重要。
Child Neuropsychol. 2021 Jul;27(5):587-600. doi: 10.1080/09297049.2021.1876010. Epub 2021 Feb 3.
4
Basal Serum Thyroxine Level should Guide Initial Thyroxine Replacement Dose in Neonates with Congenital Hypothyroidism.基础血清甲状腺素水平应指导先天性甲状腺功能减退症新生儿的初始甲状腺素替代剂量。
J Clin Res Pediatr Endocrinol. 2021 Aug 23;13(3):269-275. doi: 10.4274/jcrpe.galenos.2020.2020.0194. Epub 2020 Dec 30.
5
Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology.先天性甲状腺功能减退症:2020-2021 年共识指南更新——一项由 ENDO-欧洲参考网络倡议发起并得到欧洲儿科内分泌学会和欧洲内分泌学会认可的倡议。
Thyroid. 2021 Mar;31(3):387-419. doi: 10.1089/thy.2020.0333.
6
Performance in motor, communicative and cognitive skills of girls with congenital hypothyroidism treated from the neonatal period.新生儿期开始治疗的先天性甲状腺功能减退症女孩的运动、交流和认知技能表现。
Codas. 2020 Feb 10;32(1):e20190017. doi: 10.1590/2317-1782/20192019017. eCollection 2020.
7
White matter microstructural abnormalities in children with severe congenital hypothyroidism.儿童严重先天性甲状腺功能减退症的脑白质微观结构异常。
Neuroimage Clin. 2019;24:101980. doi: 10.1016/j.nicl.2019.101980. Epub 2019 Aug 10.
8
Evaluation and management of the child with hypothyroidism.儿童甲状腺功能减退症的评估和管理。
World J Pediatr. 2019 Apr;15(2):124-134. doi: 10.1007/s12519-019-00230-w. Epub 2019 Feb 8.
9
Intelligence Quotient at the Age of Six years of Iranian Children with Congenital Hypothyroidism.伊朗先天性甲状腺功能减退症患儿6岁时的智商
Indian Pediatr. 2018 Feb 15;55(2):121-124. Epub 2017 Sep 26.
10
Fine motor skills and expressive language: a study with children with congenital hypotyreoidism.精细运动技能与表达性语言:一项针对先天性甲状腺功能减退症患儿的研究。
Codas. 2017 Mar 9;29(1):e20160064. doi: 10.1590/2317-1782/20172016064.