01526cam a2200265 a 4500003000900000005001700009008004100026040002800067041000800095100004000103245021400143246011000357260005900467300004300526502008700569520032400656530002200980653002801002653003001030653002601060700004801086700004801134700004501182856003301227EG-GiCUC20250223030946.0140324s2013    ua dh  f m    000 0 eng d  aEG-GiCUCbengcEG-GiCUC0 aeng0 aRasha Helmy Mohamed Mohamed Elgendi10aRenal and retinal involvement in patients with bardet-biedl syndrome / cRasha Helmy Mohamed Mohamed Elgendi ; Supervised Neveen Abdelmonem Soliman , Marwa Mohamed Ibrahim Nabhan , Dina Mohamed Saied Elfayoumi15aدراسة تاثير الكلى وشبكية العين فى مرضى متلازمة باردت بيدل  aCairo : bRasha Helmy Mohamed Mohamed Elgendi , c2013  a84 P. : bcharts , facsimiles ; c25cm  aThesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics  aBackground : Bardet - biedl syndrome (BBS) is an autosomal recessive condition characterized by renal dysfunction rod- cone dystrophy postaxial polydactyly , obesity mental reardation and hypogonadism as a major criteria . Secondary features of BBS include speech delay strabismus , cataracts , brachydactyly syndactyly  aIssued also as CD 4aBardet- biedl  syndrome 4aEnd stage kidney disease  4aRetinitis pigmentosa 0 aDina Mohamed Saied Elfayoumi , eSupervisor0 aMarwa Mohamed Ibrahim Nabhan , eSupervisor0 aNeveen Abdelmonem Soliman , eSupervisor  uhttp://172.23.153.220/th.pdf