Bardet Biedl syndrome - report of a very rare case
Bardet Biedl Syndrome is a autosomal recessive condition with a wide spectrum of clinical features. The principal manifestations of the syndrome are Post axial Polydactyly, Retinitis Pigmentosa, truncal obesity, hypogonadism & renal dysfunction. The authors report a case of Bardet Biedl Syndrome...
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| 格式: | 图书 |
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Wolters Kluwer Medknow Publications,
2016-01-01T00:00:00Z.
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| 索引号: |
A1234.567 |
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