No CrossRef data available.
Published online by Cambridge University Press: 01 August 2014
The prevention of hereditary diseases after birth is essentially based on the detection of these diseases at their preclinical level. This may be made possible through a careful pedigree examination and possible identification of a “genealogical alarm”, as well as a detailed clinical examination of the subject and possible identification of preclinical signs of the pathogenesis, i.e., of a “clinical alarm”. The respective roles of chronogenetics and of gemellology in this approach are reviewed.
Lecture given at the International Conference of Medical Genetics devoted to “Preventable Aspects of Genetic Morbidity” held in Cairo, Egypt, in April 1978.