Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family.
Open Access
- 1 August 1978
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 15 (4), 288-291
- https://doi.org/10.1136/jmg.15.4.288
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.This publication has 5 references indexed in Scilit:
- Genetic and environmental interactionsCancer, 1977
- Genetic and clinical aspects of Charcot‐Marie‐Tooth's diseaseClinical Genetics, 1974
- Familial jaw cysts in Charcot-Marie-Tooth disease.Journal of Medical Genetics, 1969
- Linkage analysis of the nevoid basal cell carcinoma syndromeAnnals of Human Genetics, 1968
- The 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 parathormoneCancer, 1965