Klin Padiatr 2001; 213(1): 8-12
DOI: 10.1055/s-2001-11265
ORIGINALARBEIT

Georg Thieme Verlag Stuttgart · New York

Bardet-Biedl-Syndrom: nephrourologische und humangenetische Aspekte

Bardet-Biedl syndrome - aspects of nephro-urology and human genetics.P.  Brühl1 , G.  Schwanitz2 , R.  Mallmann3 , S.  C.  Müller1 , R.  Raff 2
  • 1Urologische Klinik u. Poliklinik,
  • 2Institut für Humangenetik,
  • 3Zentrum für Kinderheilkunde, Pädiatrische Nephrologie der Universität Bonn
Further Information

Publication History

Publication Date:
31 December 2001 (online)

Zusammenfassung.

Beim Bardet-Biedl-Syndrom handelt es sich um einen genetisch heterogenen Merkmalskomplex mit autosomal-rezessivem Erbgang, bei dem bisher fünf Gen-Loci beschrieben sind. Die Diagnose dieses Syndroms beruht auf den Hauptmanifestationen Hypogenitalismus, altersabhängige, zunehmende Adipositas und renale Funktionsminderung, altersabhängige, fortschreitende Retinadegeneration mit möglicher Erblindung sowie postaxiale Polydaktylie und geistige Behinderung. Die Lebenserwartung ist eingeschränkt. Es werden Probleme der Frühdiagnostik, des sekundären Hyperparathyreoidismus sowie Fragen der operativen genitalen Rekonstruktion und der Nierenersatztherapie besprochen.

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.

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Prof. Dr. Peter Brühl

Klinik und Poliklinik für Urologie der Universität Bonn

Sigmund-Freud-Str. 25

53105 Bonn

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