Loading...
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...
Saved in:
| Main Authors: | , , , , |
|---|---|
| Format: | Artigo |
| Language: | Inglês |
| Published: |
BioMed Central
2011
|
| Subjects: | |
| Online Access: | 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 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|