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Lint: neuroferritinopathy

neuroferritinopathy
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"Neuroferritinopathy, also known as neurodegeneration with brain iron accumulation type 2 (NBIA type 2), is a disorder of iron metabolism caused by a mutation in the ferritin light chain 1 gene (FTL1) on chromosome 19."

Line 1:263 · Italics should be used only in exceptional circumstances: '<em>FTL1</em>'
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"T2/FLAIR: hyperintensity in the globus pallidi and putamina, caudate, substantia nigra, and cerebellar nuclei, these are reflective of cystic changes 3"

Line 17:1 · Generally, don't use bold in text: '<strong>T2/FLAIR</strong>'

"T1: hypointense ring surrounding aforementioned cystic changes 3"

Line 20:1 · Generally, don't use bold in text: '<strong>T1</strong>'

"GRE/SWI: markedly hypointense ring surrounding aforementioned cystic changes 3"

Line 23:1 · Generally, don't use bold in text: '<strong>GRE/SWI</strong>'
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