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锁骨颅骨发育不全中的牙齿成熟延迟。

Delayed dental maturation in cleidocranial dysplasia.

作者信息

Shaikh R, Shusterman S

机构信息

Pediatric Dentistry, Eastman Dental Center, Rochester, New York, USA.

出版信息

ASDC J Dent Child. 1998 Sep-Oct;65(5):325-9, 355.

PMID:9795736
Abstract

Cleidocranial dysplasia (CCD), a rare, inherited, generalized, skeletal and dental dysplasia, exhibiting an autosomal dominant mode of transmission, may be associated with delays during tooth maturation. To test whether permanent tooth formation is delayed in patients with CCD and if the presence of supernumerary teeth adversely influences maturation of the dentition, a group of CCD patients (eight females, three males) was compared to an equal number of control subjects matched for age and gender. Dental maturity was assessed using panoramic radiographs and the Dental Maturity Ratio, (DMR = mean dental age divided by the chronological age) was calculated. The mean DMR in CCD patients (0.87 +/- 0.14) was lower than in the control group (1.06 +/- 0.14), p < 0.01. Among patients with CCD, patients with supernumerary teeth, had a lower DMR (0.82 +/- 0.13 vs. 0.91 +/- 0.16), but the difference did not reach statistical significance. After adjusting for the presence of supernumerary teeth the diagnosis of CCD was still found to be associated with lower DMR than controls, p = 0.0569. We conclude that CCD patients have delayed tooth development of approximately 2.1 years and that among these patients, those with supernumerary teeth were further delayed by 1.5 years.

摘要

锁骨颅骨发育不全(CCD)是一种罕见的、遗传性的、全身性骨骼和牙齿发育异常疾病,呈常染色体显性遗传模式,可能与牙齿成熟延迟有关。为了测试CCD患者恒牙形成是否延迟,以及多生牙的存在是否会对牙列成熟产生不利影响,将一组CCD患者(8名女性,3名男性)与同等数量、年龄和性别匹配的对照受试者进行比较。使用全景X线片评估牙齿成熟度,并计算牙齿成熟率(DMR = 平均牙齿年龄除以实际年龄)。CCD患者的平均DMR(0.87±0.14)低于对照组(1.06±0.14),p < 0.01。在CCD患者中,有多生牙的患者DMR较低(0.82±0.13对0.91±0.16),但差异未达到统计学意义。在调整多生牙的存在后,仍发现CCD的诊断与低于对照组的DMR相关,p = 0.0569。我们得出结论,CCD患者的牙齿发育延迟约2.1年,在这些患者中,有多生牙的患者进一步延迟1.5年。

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