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Inbreeding in recessive diseases.

作者信息

Tchen P, Bois E, Feingold J, Feingold N, Kaplan J

出版信息

Hum Genet. 1977 Sep 22;38(2):163-7. doi: 10.1007/BF00527398.

DOI:10.1007/BF00527398
PMID:302820
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% albinism: 5.0% achromatopsia: 12.5% (Albinism and spinal muscular atrophy are heterogeneous conditions). The increase in the frequency of first cousin marriage 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.

摘要

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本文引用的文献

1
The incidence of consanguineous matings in Japan, with remarks on the estimation of comparative gene frequencies and the expected rate of appearance of induced recessive mutations.日本近亲交配的发生率,兼论比较基因频率的估计及诱发隐性突变的预期出现率
Am J Hum Genet. 1949 Dec;1(2):156-78.
2
FAMILIAL JUVENILE NEPHRONOPHTHISIS. AN UNRECOGNIZED RENAL DISEASE IN THE UNITED STATES.家族性青少年肾单位肾痨。美国一种未被认识的肾脏疾病。
Pediatrics. 1964 Sep;34:337-45.
3
Familial juvenile nephronophthisis.
Acta Paediatr (Stockh). 1962 Sep;51:561-74. doi: 10.1111/j.1651-2227.1962.tb06582.x.
4
Frequencies of pedigrees of consanguineous marriages and mating structure of the population.
Ann Hum Genet. 1962 May;25:347-77. doi: 10.1111/j.1469-1809.1962.tb01772.x.
5
Juvenile nephronophthisis. Part 1. A genetically determined nephropathy with hypotonic polyuria and azotaemia.
Acta Paediatr (Stockh). 1960 Jul;49:470-9. doi: 10.1111/j.1651-2227.1960.tb07761.x.
6
The probability of consanguineous marriages.近亲结婚的概率。
Genetics. 1966 Jul;54(1):37-60. doi: 10.1093/genetics/54.1.37.
7
Distance and kinship in northeastern Brazil.巴西东北部的距离与亲属关系。
Am J Hum Genet. 1969 Jan;21(1):1-22.
8
Albinism.白化病。
Adv Hum Genet. 1971;2:61-142.
9
The genetic identity of acute infantile spinal muscular atrophy.急性婴儿脊髓性肌萎缩症的基因特征
Brain. 1973 Sep;96(3):463-70. doi: 10.1093/brain/96.3.463.
10
Genetic structure of Switzerland.瑞士的基因结构。
Am J Hum Genet. 1973 Jul;25(4):347-61.