中华皮肤科杂志 ›› 2025, Vol. 58 ›› Issue (2): 175-177.doi: 10.35541/cjd.20220781

• 病例报告 • 上一篇    下一篇

新发GNAS基因突变致婴儿板层样皮肤骨瘤伴局限性脱发1例

吴邓婷1    何瑞2    杨思燕1    张嫦娥1    马琳2    张斌2   

  1. 1郑州大学附属儿童医院  河南省儿童医院郑州儿童医院皮肤科,郑州  450018;2国家儿童医学中心  首都医科大学附属北京儿童医院皮肤科,北京  100045
  • 收稿日期:2022-11-07 修回日期:2023-11-27 发布日期:2025-02-07
  • 通讯作者: 张斌 E-mail:dr.binzhang@163.com
  • 基金资助:
    北京市自然科学基金(7222058);河南省儿科疾病临床医学研究中心开放课题(YJZX202209);国家区域医疗中心开放课题(NRMC0101);国家重点研发计划项目(2023YFC2508200)

A case of infantile plate-like osteoma cutis complicated by focal alopecia caused by a novel mutation in the GNAS gene

Wu Dengting1, He Rui2, Yang Siyan1, Zhang Chang′e1, Ma Lin2, Zhang Bin2   

  1. 1Department of Dermatology, Children′s Hospital Affiliated of Zhengzhou University, Henan Children′s Hospital, Zhengzhou Children′s Hospital, Zhengzhou 450018, China; 2Department of Dermatology, Beijing Children′s Hospital, Capital Medical University, National Center for Children′s Health, Beijing 100045, China
  • Received:2022-11-07 Revised:2023-11-27 Published:2025-02-07
  • Contact: Zhang Bin E-mail:dr.binzhang@163.com
  • Supported by:
    Beijing Municipal Natural Science Foundation (7222058); The Open Project of Henan Clinical Research Center of Childhood Diseases (YJZX202209); National Regional Medical Center Opening Project (NRMC0101); National Key Research and Development Program of China(2023YFC2508200)

摘要: 患儿男,4个月15天。因出生时即有左前胸及头皮质硬皮损伴脱发就诊,头皮皮损因表面头发稀疏而发现。患儿系第1胎第1产,36+1W早产、剖宫产,无宫内发育迟缓,无窒息史;出生时无外伤及传染病史;父母体健,非近亲结婚,家族中无类似病史……

引用本文

吴邓婷 何瑞 杨思燕 张嫦娥 马琳 张斌. 新发GNAS基因突变致婴儿板层样皮肤骨瘤伴局限性脱发1例[J]. 中华皮肤科杂志, 2025,58(2):175-177. doi:10.35541/cjd.20220781

Wu Dengting, He Rui, Yang Siyan, Zhang Chang′e, Ma Lin, Zhang Bin. A case of infantile plate-like osteoma cutis complicated by focal alopecia caused by a novel mutation in the GNAS gene[J]. Chinese Journal of Dermatology, 2025, 58(2): 175-177.doi:10.35541/cjd.20220781