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An interesting case of familial chylomicronemia syndrome in a cleft palate child
Familial chylomicronemia syndrome is a very rare condition with an incidence of one in one million. We report such a condition detected incidentally in a cleft child.
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Medknow Publications
2008
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2739552/ https://ncbi.nlm.nih.gov/pubmed/19753206 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0970-0358.41116 |
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