hereditary amyloidosis


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Related to hereditary amyloidosis: Hereditary hemochromatosis, ATTR amyloidosis

fa·mil·i·al am·y·loid neu·rop·a·thy

[MIM*105120, various kinds]
a disorder in which various peripheral nerves are infiltrated with amyloid and their functions disturbed; an abnormal prealbumin is also formed and is present in the blood; characteristically, it begins during midlife and is found largely in patients of Portuguese descent; autosomal dominant inheritance. Other rare clinical types occur.
Synonym(s): familial amyloidosis, hereditary amyloidosis

hereditary amyloidosis

Metabolic disease Any of the usually AD conditions caused by tissue accumulation of defective amyloid proteins in the brain, heart and kidneys. See Amyloidosis.
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References in periodicals archive ?
116-119) A few non-AA cases have properties of hereditary amyloidosis.
The clinical and biochemical spectrum of hereditary amyloidosis.
End-stage disease and dialysis in hereditary amyloidosis TTR V30M: presentation, survival and prognostic factors.
A proposed histopathologic classification, scoring, and grading system for renal amyloidosis: standardization of renal amyloid biopsy report
ATTR, amyloidosis derived from a variant of transthyretin, is the most common hereditary amyloidosis in the United States and worldwide.
Successful hepatorenal transplantation in hereditary amyloidosis caused by frame-shift mutation in fibrinogen A alpha-chain gene.
Amyloidosis--where are we now and where are we heading?

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