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[Autosomal-dominant osteopetrosis in Chuvashiya].

作者信息

Ginter E K, Kirillov A G, Rogaev E I

机构信息

Medical Genetic Research Center, Russian Academy of Medical Sciences, Moscow, 115478 Russia.

出版信息

Genetika. 2001 Aug;37(8):1152-5.

Abstract

A genetic epidemiological study of osteopetrosis was carried out in Chuvashiya. The major signs of this disorder are severe anemia developed in the prenatal or early postnatal life, hepatosplenomegaly, and a progressive loss of sight and hearing. Osteopetrosis showed the autosomal recessive inheritance with a somewhat increased proportion of affected patients in families. The lowest estimate of osteopetrosis frequency in Chuvashiya was 0.00026, one affected patient per 3879 newborns. The osteopetrosis gene occurred at a frequency of 0.016; the proportion of heterozygotes was 3.15%. The gene was shown to be evenly distributed throughout the republic.

摘要

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