Two Brothers with Bardet-Biedl Syndrome Presenting with Chronic Renal Failure
Bardet-Biedl Syndrome (BBS) is a rarely seen autosomal recessive transfer disease characterised by retinal dystrophy, obesity, extremity deformities, mental retardation, and renal and genital system anomalies. BBS shows heterogenic transfer. To date, 18 genes (BBS1–18) and 7 BBS proteins have been d...
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Main Authors: | Cem Sahin, Bulent Huddam, Gulhan Akbaba, Hasan Tunca, Emine Koca, Mustafa Levent |
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Format: | Article |
Language: | English |
Published: |
Wiley
2015-01-01
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Series: | Case Reports in Nephrology |
Online Access: | http://dx.doi.org/10.1155/2015/764973 |
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