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Alstrom syndrome (OMIM 203800): a case report and literature review
BACKGROUND: Alstrom syndrome (AS) is a rare autosomal recessive disease characterized by multiorgan dysfunction. The key features are childhood obesity, blindness due to congenital retinal dystrophy, and sensorineural hearing loss. Associated endocrinologic features include hyperinsulinemia, early-o...
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| Hauptverfasser: | , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2007
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2266715/ https://ncbi.nlm.nih.gov/pubmed/18154657 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-2-49 |
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