Bardet-Biedl Syndrome: A Rare Entity
Bardet-Biedl syndrome (BBS) is a rare ciliopathy autosomal recessive hereditary disorder due to mutation in 14 genes. It affects multiple organ systems such as renal dysfunction, congenital heart disease, ocular defect, cognitive impairment, and speech disorder and presented clinically as truncal ob...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Jaypee Brothers Medical Publisher
2022-08-01
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| Series: | Journal of South Asian Association of Pediatric Dentistry |
| Subjects: | |
| Online Access: | https://www.jsaapd.com/doi/JSAAPD/pdf/10.5005/jp-journals-10077-3224 |
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