A child with hyperferritinemia: Case report

• मुख्य लेखकों: Sandri Alessandro (लेखक), Roetto Antonella (लेखक), Longo Filomena (लेखक), Serra Melania (लेखक), Piga Antonio (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: BMC, 2011-05-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: Connect to this object online.

<p>Abstract</p> <p>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...