AMELOGENESIS IMPERFECTA AMONG ISRAELI JEWS AND THE DESCRIPTION OF A NEW TYPE OF LOCAL HYPOPLASTIC AUTOSOMAL RECESSIVE AMELOGENESIS IMPERFECTA

被引:68
作者
CHOSACK, A [1 ]
EIDELMAN, E [1 ]
WISOTSKI, I [1 ]
COHEN, T [1 ]
机构
[1] HEBREW UNIV JERUSALEM,FAC MED,DEPT HUMAN GENET,JERUSALEM 91000,ISRAEL
来源
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS | 1979年 / 47卷 / 02期
关键词
D O I
10.1016/0030-4220(79)90170-1
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Amelogenesis imperfecta (Al) was detected in ine of 70,359 school children surveyed, a prevalence approximating 1:8,000. Of these cases, eight were of the hypoplastic type and one the snow-capped hypomaturation type. Family studies demonstrated that hypoplastic Al was an autosomal dominant trait in two children and an autosomal recessive in six. Of three additional families referred to our clinic, two had autosomal recessive hypoplastic Al and one the hypocalcified type, inherited as an autosomal dominant trait. In four families, a new type of local hypoplastic autosomal recessive Al was observed, characterized by horizontal pitting and grooving more pronounced in the middle third of the crowns of most teeth in both dentitions. © 1979.
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页码:148 / 156
页数:9
相关论文
共 13 条
[1]  
COHEN T, 1971, ISRAEL J MED SCI, V7, P1509
[2]   SOME OBSERVATIONS ON AMELOGENESIS IMPERFECTA AND CALCIFICATION OF THE DENTAL ENAMEL [J].
DARLING, AI .
PROCEEDINGS OF THE ROYAL SOCIETY OF MEDICINE-LONDON, 1956, 49 (10) :759-765
[3]  
PINDBORG JJ, 1970, PATHOLOGY DENTAL HAR, P77
[4]   HEREDITARY ENAMEL DEFECTS [J].
RUSHTON, MA .
PROCEEDINGS OF THE ROYAL SOCIETY OF MEDICINE-LONDON, 1964, 57 (01) :53-58
[5]  
Schulze C, 1957, ACTA GENET, V7, P23
[6]  
STERN C, 1973, PRINCIPLES HUMAN GEN, P204
[7]   HEREDITARY DISTURBANCES OF ENAMEL FORMATION AND CALCIFICATION [J].
WEINMANN, JP ;
SVOBODA, JF ;
WOODS, RW .
JOURNAL OF THE AMERICAN DENTAL ASSOCIATION, 1945, 32 (07) :397-418
[8]  
WINTER G B, 1969, British Dental Journal, V127, P157
[9]  
WITKOP C J, 1957, Acta Genet Stat Med, V7, P236
[10]  
Witkop C. J, 1976, ORAL FACIAL GENETICS, P151