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Nevoid basal cell carcinoma syndrome: review of 118 affected individuals.
- Source :
-
American journal of medical genetics [Am J Med Genet] 1994 Apr 15; Vol. 50 (3), pp. 282-90. - Publication Year :
- 1994
-
Abstract
- 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.
- Subjects :
- Abnormalities, Multiple genetics
Adolescent
Adult
Age of Onset
Alleles
Australia epidemiology
Bone and Bones abnormalities
Calcinosis genetics
Child
Child, Preschool
Chromosome Mapping
Chromosomes, Human, Pair 9
Dura Mater pathology
Female
Genetic Linkage
Genetic Testing
Humans
Infant
Jaw Diseases genetics
Keratoderma, Palmoplantar genetics
Male
Middle Aged
Mutation
New Zealand epidemiology
Odontogenic Cysts genetics
Palate abnormalities
Phenotype
Prevalence
Wales epidemiology
Basal Cell Nevus Syndrome diagnosis
Basal Cell Nevus Syndrome epidemiology
Basal Cell Nevus Syndrome genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0148-7299
- Volume :
- 50
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- American journal of medical genetics
- Publication Type :
- Academic Journal
- Accession number :
- 8042673
- Full Text :
- https://doi.org/10.1002/ajmg.1320500312