Literature DB >> 3706293

Primary amyloidosis (AL) in families.

M A Gertz, J P Garton, R A Kyle.   

Abstract

We report the occurrence of immunoglobulin-related amyloidosis (AL) in three separate families, each family having two members affected. None of the six patients had evidence to suggest the presence of familial amyloidosis (AF). Previously, immunoglobulin-related amyloidosis (AL) was considered to be a sporadic disease process. Because of the occasional familial occurrence of other monoclonal gammopathies such as monoclonal gammopathy of undetermined significance, multiple myeloma, and macroglobulinemia of Waldenström, amyloidosis (AL) should be added to the list of immunopathies with a familial predisposition.

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Year:  1986        PMID: 3706293     DOI: 10.1002/ajh.2830220210

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  2 in total

1.  A father and his son with systemic AL amyloidosis.

Authors:  Stina Enqvist; Ulf-Henrik Mellqvist; Johan Mölne; Knut Sletten; Charles Murphy; Alan Solomon; Fred J Stevens; Per Westermark
Journal:  Haematologica       Date:  2009-01-27       Impact factor: 9.941

2.  Case report: Two sisters with light-chain cardiac amyloidosis, a mere coincidence?

Authors:  Sarah Cappuyns; Matthias Verbesselt; Alexander Van De Bruaene; Jan Bogaert; Lucienne Michaux; Michel Delforge
Journal:  Eur Heart J Case Rep       Date:  2022-02-17
  2 in total

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