Loading...
Bardet–Biedl Syndrome in an Ethiopian
Bardet–Biedl syndrome (BBS) is a rare familial and multi-system disorder with an autosomal recessive pattern of inheritance and wide range of clinical variability. Its main manifestations are progressive retinal dystrophy, renal dysfunction, post-axial polydactyly, central obesity, mental retardatio...
Saved in:
| Published in: | Int Med Case Rep J |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Dove
2021
|
| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7989368/ https://ncbi.nlm.nih.gov/pubmed/33776488 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/IMCRJ.S299421 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|