CLINICAL FINDINGS IN 2 AFRICAN-AMERICAN FAMILIES WITH THE NEVOID BASAL-CELL CARCINOMA SYNDROME (NBCC)

被引:40
作者
GOLDSTEIN, AM
PASTAKIA, B
DIGIOVANNA, JJ
POLIAK, S
SANTUCCI, S
KASE, R
BALE, AE
BALE, SJ
机构
[1] NCI,DERMATOL BRANCH,BETHESDA,MD 20892
[2] NCI,CLIN EPIDEMIOL BRANCH,BETHESDA,MD 20892
[3] NIH,CLIN CTR,DEPT RADIOL 2,BETHESDA,MD 20892
[4] WESTAT CORP,ROCKVILLE,MD
[5] YALE UNIV,SCH MED,DEPT GENET,NEW HAVEN,CT 06510
[6] NIAMSD,SKIN BIOL LAB,GENET STUDIES SECT,BETHESDA,MD
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 50卷 / 03期
关键词
NEVOID BASAL CELL CARCINOMA SYNDROME (NBCC); AFRICAN-AMERICANS; CLINICAL FINDINGS;
D O I
10.1002/ajmg.1320500311
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The nevoid basal cell carcinoma syndrome (NBCC) is an autosomal dominant multi-system disorder with variable expressivity. We present the clinical findings on 11 African-American NBCC cases from 2 families and a review of the literature of NBCC in African-Americans. The 2 new families, as well as those previously reported, suggest minimal expression of the basal cell carcinomas and full expression of the other components of the syndrome. The 3 most common findings in the 11 cases were jaw cysts, palmar and/or plantar pits, and calcification of the falx cerebri. Only 44% (4/11) of these cases had one or more confirmed basal cell carcinomas. This frequency is substantially less than that observed in whites (90% with basal cell carcinomas). The relative lack of these skin tumors in African-Americans partly reflects ultraviolet radiation protection resulting from increased skin pigmentation. Future research should help identify the specific mutation(s) in blacks as well as other modifying genes and environmental exposures that may contribute to the varied manifestations of the syndrome. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:272 / 281
页数:10
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