NEVOID BASAL-CELL CARCINOMA SYNDROME - REVIEW OF 118 AFFECTED INDIVIDUALS

被引:220
作者
SHANLEY, S
RATCLIFFE, J
HOCKEY, A
HAAN, E
OLEY, C
RAVINE, D
MARTIN, N
WICKING, C
CHENEVIXTRENCH, G
机构
[1] ROYAL CHILDRENS HOSP,DEPT RADIOL,BRISBANE,AUSTRALIA
[2] KING EDWARDS MEM HOSP,PERTH,AUSTRALIA
[3] ADELAIDE CHILDRENS HOSP INC,ADELAIDE,SA 5006,AUSTRALIA
[4] MATER MISERICORDIAE MOTHERS HOSP,BRISBANE,AUSTRALIA
[5] MURDOCH INST,MELBOURNE,AUSTRALIA
[6] ROYAL BRISBANE HOSP,DEPT PATHOL,BRISBANE,QLD 4029,AUSTRALIA
[7] UNIV QUEENSLAND,CTR MOLEC BIOL & BIOTECHNOL,ST LUCIA,QLD 4067,AUSTRALIA
[8] UNIV NEWCASTLE UPON TYNE,DIV HUMAN GENET,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLAND
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 50卷 / 03期
关键词
NEVOID BASAL CELL CARCINOMA SYNDROME; TUMOR SUPPRESSOR GENE; GORLIN SYNDROME; BASAL CELL NEVUS SYNDROME; ANTICIPATION; MUTATION; PITTING; BASAL CELL CARCINOMAS; KERATOCYSTS; FALCINE CALCIFICATION; IMPRINTING;
D O I
10.1002/ajmg.1320500312
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
One hundred eighteen cases of nevoid basal cell carcinoma syndrome (NBCCS, Gorlin's syndrome or basal cell nevus syndrome) are presented in this study. In aiming to ascertain all the affected families in Australia, we have examined the largest series to date. Relative frequencies of associated complications are presented and compared with those of the recent English survey by Evans et al. [J Med Genet 30:460-464, 1993]. The frequencies of most manifestations are similar. However, one major difference is that the multiple basal cell carcinomas are manifest from an earlier age in the Australian population, which probably reflects greater exposure to ultraviolet radiation. Of the 64 families ascertained, 37 represented simplex cases, and, accordingly, the apparent new mutation rate is surprisingly high (14-81%) given the lack of impact of NBCCS on reproductive capabilities. There is some evidence to suggest that this may be attributable to anticipation. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:282 / 290
页数:9
相关论文
共 20 条
[1]  
CHENEVIXTRENCH G, 1993, AM J HUM GENET, V53, P760
[2]   COMPLICATIONS OF THE NEVOID BASAL-CELL CARCINOMA SYNDROME - RESULTS OF A POPULATION-BASED STUDY [J].
EVANS, DGR ;
LADUSANS, EJ ;
RIMMER, S ;
BURNELL, LD ;
THAKKER, N ;
FARNDON, PA .
JOURNAL OF MEDICAL GENETICS, 1993, 30 (06) :460-464
[3]  
EVANS DGR, 1991, BRIT J CANCER, V64, P9959
[4]   LOCATION OF GENE FOR GORLIN SYNDROME [J].
FARNDON, PA ;
DELMASTRO, RG ;
EVANS, DGR ;
KILPATRICK, MW .
LANCET, 1992, 339 (8793) :581-582
[5]  
FEINGOLD M, 1974, D OAS, V10, P7
[6]   DEVELOPMENTAL DEFECTS IN GORLIN SYNDROME RELATED TO A PUTATIVE TUMOR SUPPRESSOR GENE ON CHROMOSOME-9 [J].
GAILANI, MR ;
BALE, SJ ;
LEFFELL, DJ ;
DIGIOVANNA, JJ ;
PECK, GL ;
POLIAK, S ;
DRUM, MA ;
PASTAKIA, B ;
MCBRIDE, OW ;
KASE, R ;
GREENE, M ;
MULVIHILL, JJ ;
BALE, AE .
CELL, 1992, 69 (01) :111-117
[7]   MULTIPLE NEVOID BASAL-CELL EPITHELIOMA, JAW CYSTS AND BIFID RIB - A SYNDROME [J].
GORLIN, RJ ;
GOLTZ, RW .
NEW ENGLAND JOURNAL OF MEDICINE, 1960, 262 (18) :908-912
[8]  
GORLIN RJ, 1987, MEDICINE, V66, P96
[9]  
HALL JG, 1990, AM J HUM GENET, V46, P857
[10]  
HOWELL JB, 1959, ARCH DERMATOL SYPH B, V28, P162