Review articles
Hematology. 2021;26:896-903Ferritin L-subunit gene mutation and hereditary
hyperferritinaemia cataract syndrome (HHCS): a
case report and literature review
Clin Chem Lab Med. 2019;57:1837-1845Hereditary hyperferritinaemia-cataract syndrome (HHCS) – an underestimated condition: ferritin light chain variant spectrum in German families
Clinical practice guidelines
None available
Online evidence-based resources
DynaMedA rigorous evidence-based point-of-care tool, can access overview and recommendations section without subscription
UpToDateRelies heavily on expert opinion. Not accessible without subscription