[低磷儿童的牙科研究]。

M Takagi, M Takahashi, S Shimooka
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引用次数: 0

摘要

低磷酸症是一种以先天性组织碱性磷酸酶缺乏为特征的遗传性疾病。它的牙齿特征之一是脱落的牙齿。我们经历了一个病例被转介到我们的诊所,主诉是下乳中切牙的丢失和脱落,在儿科诊所的血液学检查结果被诊断为高度怀疑磷酸酶缺失。经过近两年半的全身和口腔检查,以及对病程变化的进一步研究,得出以下结论:低血清碱性磷酸酶水平和高钙血症是该病的全身性表现。2. 在腕骨年龄方面没有延迟骨化。3.x线头颅造影显示,除了额部和下颌骨缺乏发育外,没有特别的头部异常。4. 牙齿发现包括明显的吸收上牙槽骨在前牙区域和明显的前乳牙不稳定。5. 对于口腔症状的变化,由于明显的不稳定而拔出A,随后A自发脱落,大约一年后,由于明显的不稳定而拔出A。撰写本文时,A稍不稳定,其他牙齿未见异常。6. 拔牙的病理组织学检查显示,拔牙后牙根端骨水泥和牙周组织有少量吸收,无明显组织变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Dental study of hypophosphatasic child].

Hypophosphatasia is a hereditary disease characterized by congenital deficiency of tissue alkaline phosphatase. One of its dental features is the shedding of teeth. We have experienced a case which was referred to our clinic with the chief complaints of loss and shedding of lower deciduous central incisors and was diagnosed to be highly suspected of hypophosphatasia as a result of hematological examination at the pediatric clinic. As a result of close systemic and dental examination and further study of changes in the course for two and a half years, the following findings were obtained: 1. Low serum alkaline phosphatase level and hypercalcemia were the systemic findings of the disease. 2. There was no delayed ossification in terms of carpal bone age. 3. X-ray cephalography revealed no particular cephalic abnormality, except the lack of development of frontalis and mandibular. 4. Dental findings comprised marked resorption of upper alveolar bone in the front teeth area and pronounced instability of front deciduous teeth. 5. As for changes in oral symptoms, extraction of A because of pronounced instability was followed by spontaneous shedding of A. About one year later, A was extracted because of marked instability. At the time of this writing, A was slightly instable without any abnormality in the other teeth. 6. Pathohistological study of the extracted teeth disclosed only a little resorption of cement of root apex and dysgonic periodontium without any marked tissue changes.

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