Yüklüyor......
A child with hyperferritinemia: Case report
Hereditary hyperferritinemia cataract syndrome (HHCS) is a rare condition caused by mutations in the gene coding for the light chain of ferritin; it does not lead to iron overload, but it is associated with the risk of developing a bilateral nuclear cataract also in childhood. On the contrary, a rai...
Kaydedildi:
| Asıl Yazarlar: | , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2011
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3113735/ https://ncbi.nlm.nih.gov/pubmed/21569394 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1824-7288-37-20 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|