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Laron综合征

Laron syndrome

定义 英文原文(暂无中文)

Laron syndrome is a congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration.

别名

生长激素抵抗所致矮小

基本事实

遗传方式
常染色体隐性
发病年龄
婴儿期、新生儿期
患病率
1-9 / 1 000 000(Europe)

相关基因 1

基因名称关联类型
GHRgrowth hormone receptorDisease-causing germline mutation(s) in

临床表型 29

极常见 99–80%12

  • 面部形状异常 HP:0001999
  • 内分泌系统异常 HP:0000818
  • 鼻发育不全/未发育 HP:0009924
  • 牙齿萌出延迟 HP:0000684
  • 骨成熟延迟 HP:0002750
  • 额头高 HP:0000348
  • 鼻梁发育不全 HP:0005281
  • 小牙畸形 HP:0000691
  • 小下颌 HP:0000347
  • 严重的身材矮小 HP:0003510
  • 牙齿发育不全 HP:0009804
  • 躯干性肥胖 HP:0001956

常见 79–30%8

  • 肘部异常 HP:0009811
  • 短指(趾) HP:0001156
  • 青春期发育延迟 HP:0000823
  • 低血糖 HP:0001943
  • 阴茎发育不良 HP:0008736
  • 运动发育迟缓 HP:0001270
  • 短趾 HP:0001831
  • 眶上嵴发育不全 HP:0009891

偶见 29–5%9

  • 颅骨形态异常 HP:0000929
  • 声音异常尖锐 HP:0001620
  • 蓝巩膜 HP:0000592
  • 鼻嵴凹陷 HP:0000457
  • 高胆固醇血症 HP:0003124
  • 少汗症 HP:0000966
  • 智力障碍 HP:0001249
  • 骨关节炎 HP:0002758
  • 早衰面容 HP:0007495

近两年的全球研究 101L2

2024/08 起在 Europe PMC 检索所得,按发表时间倒序显示最近 20 篇。标题未译成中文——自动翻译需要接入 LLM 服务,尚未引入。

  • 2026-07预印本
    The Laron Syndrome Mouse Model Reveals a Potential Contribution of Methylglyoxal-Derived Glycative Stress to IGF-1-Driven Prostate Cancer Progression
    · DOI
  • 2026-07
    LARON SYNDROME. (Growth Hormone Insensitivity) Geographical distribution and relationship to the genetic defects in the growth hormone receptor gene
    The Journal of clinical endocrinology and metabolism · DOI · Europe PMC
  • 2026-06
    Comparison Between Chronological and Bone Age at Menarche in Girls with Laron Syndrome
    Children (Basel, Switzerland) · DOI · Europe PMC
  • 2026-06综述
    Real world data on rhIGF-1 therapy in children with severe primary IGF-I deficiency - The European experience
    Growth hormone & IGF research : official journal of the Growth Hormone · DOI · Europe PMC
  • 2026-06
    Alexander von Humboldt and the little women of Loja
    Growth hormone & IGF research : official journal of the Growth Hormone · DOI · Europe PMC
  • 2026-05开放获取
    Sex-specific roles of insulin-like growth factor-1, lean mass and fat mass in type 2 diabetes prevention: Mendelian randomization studies in Western and East Asian populations
    Cardiovascular diabetology. Endocrinology reports · DOI · Europe PMC
  • 2026-05开放获取
    GH-resistant (Laron) mice: gene therapy with a liver-specific GH receptor causes unbalanced upregulation of female-biased and growth-related genes
    Frontiers in endocrinology · DOI · Europe PMC
  • 2026-05系统综述综述开放获取
    Growth Hormone and Brain Regeneration: Evidence from Clinical Studies in Dementia, Traumatic Brain Injury, and Stroke: A Systematic Review
    International journal of molecular sciences · DOI · Europe PMC
  • 2026-04开放获取
    Utilization of genetic biomarkers for childhood stunting surveillance and early detection in Southeast Asia: a systematic review
    Annals of pediatric endocrinology & metabolism · DOI · Europe PMC
  • 2026-04
    Age and sexual maturation at Spermarche in boys with Laron syndrome
    Journal of pediatric endocrinology & metabolism : JPEM · DOI · Europe PMC
  • 2026-04综述
    Growth hormone receptor blockade in cancer treatment
    Growth hormone & IGF research : official journal of the Growth Hormone · DOI · Europe PMC
  • 2026-04
    Body proportion is not affected by sex in LARON syndrome
    Growth hormone & IGF research : official journal of the Growth Hormone · DOI · Europe PMC
  • 2026-04开放获取
    MCT4 deficiency suppresses tumor incidence and metastasis by downregulating IGF1 expression and enhancing anti-tumor immunity
    Communications biology · DOI · Europe PMC
  • 2026-04开放获取
    Zebrafish gon4la mutants recapitulate human GON4L-related growth disorders and reveal novel metabolic organs abnormalities
    Scientific reports · DOI · Europe PMC
  • 2026-04开放获取
    Targeting Mitochondrial Stress Responses: Terbinafine and Miglustat as Novel Lifespan and Healthspan Modulators
    Aging cell · DOI · Europe PMC
  • 2026-04荟萃分析开放获取
    Long-acting growth hormone for treating growth hormone deficiency in children: a meta-analysis of randomized controlled trials focusing on changes in body mass index
    The Journal of clinical endocrinology and metabolism · 被引 2 · DOI · Europe PMC
  • 2026-03综述
    The IGF-1 senescence switch: a biphasic model for SASP-driven aging and precision senomodulation
    Cytokine · DOI · Europe PMC
  • 2026-03
    A cartilage-targeted IGF-1-antibody fusion protein as a new therapeutic approach for IGF-1 deficiency
    Molecular therapy : the journal of the American Society of Gene Therap · DOI · Europe PMC
  • 2026-03
    Low or Low-Normal Insulin-Like Growth Factor 1 After Traumatic Brain Injury: Interpretation and Implications
    Journal of neurotrauma · DOI · Europe PMC
  • 2026-03综述开放获取
    Growth factor applications and clinical translation: advances and challenges
    Annals of medicine · DOI · Europe PMC

境外已获批用于本病的药物 1L2

欧盟 1 项、美国 0 项。同一药物在两地各批一次的,会分别列出。

「境外已获批」不等于「在中国能用」。中间隔着进口注册、临床急需境外新药通道、海南博鳌乐城国际医疗旅游先行区等几条路径,各有各的条件与费用。这一节能确定地告诉你的只有一件事:这个病在世界范围内已经有获得批准的药物,它叫什么名字。拿这个名字去问主治医生,是下一步最省力的做法。

药名一律保留英文原文,不作翻译——中国的药品通用名与英文名的音译经常不一致,译错会让人去找一个不存在的药。

已获孤儿药资格、尚未获批的在研药物(1 项)

孤儿药资格只是一种监管身份——它意味着监管机构认可这是罕见病用药并给予研发激励,不代表这个药已被证明有效,也不代表将来一定能上市。绝大多数最终不会成药。列在这里是为了看清有哪些方向正在被尝试。

  • Mecasermin欧盟2005-08-26
    Treatment of primary growth hormone insensitivity syndrome
    官方记录

数据来自欧洲药品管理局(EMA)的药品与孤儿药资格公开导出表,以及美国 FDA 孤儿药资格数据库。两边口径不同:欧盟一侧取的是当前状态仍为「已授权」的药品;美国一侧记录的是「曾获批准」这一事实,FDA 的公开表不追踪药物此后是否退市(例如 Relyvrio 于 2024 年撤市,表中仍记为已获批)。请以官方记录页为准。

在中国开展的临床试验 1L2

按病名在 ClinicalTrials.gov 检索、并校验研究中心含中国大陆而来。登记状态不等于现在真的能入组——务必按 NCT 号到原站核实,并与主治医生商量。

当前没有检索到登记为可入组的试验。

其他状态的试验(1 项)
  • 已完成NCT00368173
    IGF-I/IGFBP-3 Therapy in Children and Adolescents With Growth Hormone Insenitivity Syndrome (GHIS) Such as Laron Syndrome
    II 期、III 期 · 干预性Insmed Incorporated
    中国研究中心 1 个:Hong Kong

外部标识与链接

发现这一页有错误?告诉我 · 邮件主题会自动带上本页的 ORPHA 编号

本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)