What is another word for minkowski-chauffard syndrome?
Pronunciation: [mɪŋkˈa͡ʊskɪʃˈə͡ʊfəd sˈɪndɹə͡ʊm] (IPA) 
Minkowski-Chauffard Syndrome is a rare genetic disorder that affects the way the body metabolizes iron. This condition is also known by several other names such as hyperferritinemia-cataract syndrome and hereditary hyperferritinemia-cataract syndrome. The symptoms of this syndrome include early-onset cataracts, hyperferritinemia (increased levels of ferritin in the blood), and sometimes a mild iron overload. This disorder is inherited in an autosomal dominant pattern and is caused by mutations in the ferritin light chain (FTL) gene. While the name may vary, it is important to note that early diagnosis and treatment is essential in managing this condition.
