
Results of clinico-genetic examinations of 26 patients with hepatocerebral dystrophy and of 36 relatives of theirs was presented. The genogeography of this disease in the Bashkir Autonomous Republic was studied. It is stressed that the determination of the ceruloplasmin blood levels are not sufficiently informative for diagnosing the heterozygotic carrying. The problem of clinical polymorphism of the hepatocerebral dystrophy is discussed.
Adult, Male, Polymorphism, Genetic, Adolescent, Ceruloplasmin, Middle Aged, Pedigree, Russia, Hepatolenticular Degeneration, Ethnicity, Humans, Female, Child
Adult, Male, Polymorphism, Genetic, Adolescent, Ceruloplasmin, Middle Aged, Pedigree, Russia, Hepatolenticular Degeneration, Ethnicity, Humans, Female, Child
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