PERSPECTIVES ON CRANIOFACIAL ASYMMETRY .6. THE HAMARTOSES

被引：14
作者：
COHEN, MM [1 ]
机构：
[1] DALHOUSIE UNIV,FAC MED,DEPT PEDIAT,HALIFAX,NS B3H 3J5,CANADA
来源：
INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY | 1995年 / 24卷 / 03期
关键词：
STURGE WEBER ANGIOMATOSIS; EPIDERMAL NEVUS SYNDROME; GARDNER SYNDROME; NEUROFIBROMATOSIS; PROTEUS SYNDROME;
D O I：
10.1016/S0901-5027(06)80126-8
中图分类号：
R78 [口腔科学];
学科分类号：
1003 ;
摘要：
The hamartoses are a large group of disorders with autosomal dominant inheritance or sporadic occurrence. The genes responsible for some have been localized to specific chromosomes and in several instances, genetic heterogeneity has been established. Thus neurofibromatosis and tuberous sclerosis are no longer single entities. For example, the gene for Type I neurofibromatosis is on chromosome 17 and the gene for Type II is on chromosome 22. In this paper, genetic aspects of the hamartoses are updated and asymmetry is discussed in Sturge-Weber angiomatosis, epidermal nevus syndrome, Gardner syndrome, neurofibromatosis, and Proteus syndrome.
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页码：195 / 200
页数：6
相关论文
共 14 条
[1]  
BRUWER AJ, 1955, ARCH OPHTHALMOL-CHIC, V53, P2
[2]  
Cohen M M Jr, 1988, Neurofibromatosis, V1, P260
[3]  
Cohen M M Jr, 1979, Birth Defects Orig Artic Ser, V15, P291
[4]   PROTEUS SYNDROME - CLINICAL-EVIDENCE FOR SOMATIC MOSAICISM AND SELECTIVE REVIEW [J].
COHEN, MM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (05) :645-652
[5]   FURTHER DIAGNOSTIC THOUGHTS ABOUT THE ELEPHANT MAN [J].
COHEN, MM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 29 (04) :777-782
[6]  
COHEN MM, 1996, CHILD MULTIPLE BIRTH
[7]  
Gorlin RJ, 1990, PLAST RECONSTR SURG
[8]  
HOVELS O, 1979, MSCHR KINDERHEILKD, V127, P585
[9]  
KREIBORG S, 1991, P FINN DENT SOC, V87, P1983
[10]  
Sitzmann F, 1977, Dtsch Zahnarztl Z, V32, P781
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