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- W2079461951 abstract "Bardet-Biedl syndrome is a genetically heterogeneous autosomal recessive complex of features in which five gene loci have been described up to now. The diagnosis of this rare syndrome is based on the main manifestations hypogonadism, age-dependent increasing obesity and reduction of renal function, age-dependent progressive retinal degeneration with blindness as well as postaxial polydactyly and mental retardation. The life expectancy is short. Problems of early diagnostics, secondary hyperparathyroidism as well as surgical reconstruction of the genitals and kidney replacement therapy are discussed." @default.
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- W2079461951 date "2001-01-01" @default.
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- W2079461951 title "Bardet-Biedl-Syndrom: nephrourologische und humangenetische Aspekte" @default.
- W2079461951 doi "https://doi.org/10.1055/s-2001-11265" @default.
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