齐默尔曼-拉班德综合征和婴儿系统性阴症:一个团,有两个单独的术语,重叠的特征:一个案例报告
Fatemeh Owlia1, Alireza Navabazam2, Mohammad-Hasan Akhavan-Karbasi1
1Department of Oral and Maxillofacial Medicine, School of Dentistry, Yazd Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.
BMC pediatrics
|October 12, 2023
概括
齐默尔曼-拉班德综合征 (Zimmermann-Laband Syndrome,简称ZLS) 和婴儿系统性阴 (Infantile Systemic Hyalinosis,简称ISH) 呈现出各种症状. 这一案例突出了两者的罕见表现,强调了牙医在早期诊断中发挥的关键作用,以获得更好的患者结果.
科学领域:
- 口腔医学是指口腔医学.
- 遗传学 遗传学 是一个
- 皮肤病学 皮肤病学
背景情况:
- 齐默尔曼-拉班德综合征 (Zimmermann-Laband Syndrome,简称ZLS) 和婴儿系统性阴症 (Infantile Systemic Hyalinosis,简称ISH) 是一种罕见的遗传疾病,具有多种表现.
- 本报告详细介绍了一个独特的病例,该病例表现出ZLS和ISH的特征,由口腔医学专家和外科医生记录.
研究的目的:
- 报告一种罕见的病例,该病例呈现出齐默尔曼-拉班德综合征和婴儿系统性阴症的特征.
- 突出口腔表现在诊断罕见遗传疾病中的重要性.
主要方法:
- 一个18个月大的女性患者的病例报告.
- 在全身麻醉下手术切除牙过度生长.
- 手术后六个月的随访.
主要成果:
- 该患者出现了严重的牙过度生长,完全掩盖了突发的牙和多个乳头状皮肤病变.
- 手术干预改善了和呼吸.
- 手术后的随访显示,牙外观和相关功能问题有所改善.
结论:
- 由于临床特征含糊不清,ZLS和ISH存在诊断挑战.
- 早期诊断对于预后和管理至关重要.
- 口腔医学专家和牙医对于识别这些罕见疾病至关重要.
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