PERIODONTAL MANIFESTATION OF HYPOPHOSPHATASIA - A FAMILY CASE-REPORT

被引：21

作者：

PLAGMANN, HC ^{[1
]}

KOCHER, T ^{[1
]}

KUHRAU, N ^{[1
]}

CALIEBE, A ^{[1
]}

机构：

[1] INST HUMAN GENET & ANTHROPOL,D-24105 KIEL,GERMANY

来源：

JOURNAL OF CLINICAL PERIODONTOLOGY | 1994年 / 21卷 / 10期

关键词：

HYPOPHOSPHATASIA; PREMATURE DECIDUOUS TOOTH LOSS; ODONTOHYPOPHOSPHATASIA;

D O I：

10.1111/j.1600-051X.1994.tb00791.x

中图分类号：

R78 [口腔科学];

学科分类号：

1003 ;

摘要：

Hypophosphatasia is a rare inherited disease, the 1st clinical sign of which is often a premature loss of deciduous teeth. We describe clinical, histological and SEM findings of 2 cases of hypophosphatasia from a single family and discuss the pathological mechanisms with reference to the literature.

引用

页码：710 / 716

页数：7

共 30 条

[1]

ARMITAGE GC, 1991, PERIODONTAL DISEASES

[2] LABORATORY STUDIES OF A FAMILY MANIFESTING PREMATURE EXFOLIATION OF DECIDUOUS TEETH [J].