Abstract
A family is described in which 16 individuals in 3 generations have Charcot-Marie-Tooth disease. At least 6 family members also have the naevoid basal cell carcinoma syndrome. In addition, 1 subject with both disorders has 2 young daughters with the naevoid basal cell carcinoma syndrome.
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Selected References
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- Anderson D. E. Linkage analysis of the nevoid basal cell carcinoma syndrome. Ann Hum Genet. 1968 Oct;32(2):113–123. doi: 10.1111/j.1469-1809.1968.tb00056.x. [DOI] [PubMed] [Google Scholar]
- GORLIN R. J., VICKERS R. A., KELLEN E., WILLIAMSON J. J. MULTIPLE BASAL-CELL NEVI SYNDROME. AN ANALYSIS OF A SYNDROME CONSISTING OF MULTIPLE NEVOID BASAL-CELL CARCINOMA, JAW CYSTS, SKELETAL ANOMALIES, MEDULLOBLASTOMA, AND HYPORESPONSIVENESS TO PARATHORMONE. Cancer. 1965 Jan;18:89–104. doi: 10.1002/1097-0142(196501)18:1<89::aid-cncr2820180114>3.0.co;2-9. [DOI] [PubMed] [Google Scholar]
- Skre H. Genetic and clinical aspects of Charcot-Marie-Tooth's disease. Clin Genet. 1974;6(2):98–118. doi: 10.1111/j.1399-0004.1974.tb00638.x. [DOI] [PubMed] [Google Scholar]
- Strong L. C. Genetic and environmental interactions. Cancer. 1977 Oct;40(4 Suppl):1861–1866. doi: 10.1002/1097-0142(197710)40:4+<1861::aid-cncr2820400815>3.0.co;2-9. [DOI] [PubMed] [Google Scholar]
- Swift M. R., Horowitz S. L. Familial jaw cysts in Charcot-Marie-Tooth disease. J Med Genet. 1969 Jun;6(2):193–195. doi: 10.1136/jmg.6.2.193. [DOI] [PMC free article] [PubMed] [Google Scholar]