Inbreeding in recessive diseases
- 1 January 1977
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 38 (2) , 163-167
- https://doi.org/10.1007/bf00527398
Abstract
The consanguinity of parents (born in France) of individuals who have a recessive disease has been studied. The frequency of first cousin marriages is less than 0.2% in the general French population. Among the parents of affected individuals the following frequencies of first cousin matings were observed: cystic fibrosis: 1.4% cystinosis: 7.1% nephronophtisis: 5.6% spinal muscular atrophy: 4.5% albinsism: 5.0% achromatopsia: 12.5% (Albinism and spinal muscular atrophy are heterogeneous conditions). The increase in the frequency of first cousin marriages relative to that of the general population is much greater, as expected, in cystinosis, which is a rare disease, than in cystic fibrosis, which is the most frequent recessive disorder in France. Inbreeding in cystinosis and cystic fibrosis was also studied by computing the distance between parental birth places. This distance is smaller in cystinosis than in cystic fibrosis.Keywords
This publication has 20 references indexed in Scilit:
- Infantile cystinosis in France: genetics, incidence, geographic distribution.Journal of Medical Genetics, 1976
- [Incidence of pancreatic cystic fibrosis in France].1974
- Marital distances and inbreeding in porto alegre, BrazilSocial Biology, 1974
- Genetic structure of Switzerland.1973
- THE PROBABILITY OF CONSANGUINEOUS MARRIAGESGenetics, 1966
- A genetic study of fibrocystic disease of the pancreasAnnals of Human Genetics, 1965
- Familial Juvenile NephronophthisisActa Paediatrica, 1962
- Frequencies of pedigrees of consanguineous marriages and mating structure of the populationAnnals of Human Genetics, 1962
- Juvenile Nephronophthisis. Part I A Genetically Determined Nephropathy with Hypotonic Polyuria and AzotaemiaActa Paediatrica, 1960
- THE GENETICS OF LIGNAC-FANCONI DISEASEActa Paediatrica, 1952