Etiology
mutations in the APP gene coding for the amyloid beta A4 precursor protein (MIM.104760)
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The familial occipital calcifications, hemorrhagic strokes, leukoencephalopathy, arterial dysplasia, and dementia (FOCCHS-LADD) syndrome is a rare familial disease. MIM.605714
Etiology
mutations in the APP gene coding for the amyloid beta A4 precursor protein (MIM.104760)
MIM.605714