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 in...
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| Auteurs principaux: | , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Wolters Kluwer Medknow Publications
2016-01-01
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| Collection: | National Journal of Clinical Anatomy |
| Sujets: | |
| Accès en ligne: | http://www.njca.info/article.asp?issn=2277-4025;year=2016;volume=5;issue=4;spage=228;epage=230;aulast=Shirahatti |
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