
pmid: 7294022
pmc: PMC1685137
This paper describes a family in which 10 members of 3 generations have IgM-IgG cryoglobulinemia. Their pedigree is characteristic of autosomal dominant inheritance. No underlying disease that could account for the cryoglobulinemia has been identified in any patient, and no linkage of the cryoglobulinemia to HLA-A and -B locus haplotypes, blood group antigens, or immunoglobulin Gm allotypes has been detected. The rheumatoid factors of this kindred react with some, but not all, human IgG; however, their rheumatoid factors are not antibodies to any known human Gm or Km allotype. This family demonstrates that "essential" mixed cryoglobulinemia can be inherited, and that the clinical manifestations of an inherited cryoglobulinemia may vary among family members.
Male, Genetic Linkage, Paraproteinemias, ABO Blood-Group System, Pedigree, Major Histocompatibility Complex, Cryoglobulinemia, Immunoglobulin M, Rheumatoid Factor, Immunoglobulin G, Humans, Female, Genes, Dominant
Male, Genetic Linkage, Paraproteinemias, ABO Blood-Group System, Pedigree, Major Histocompatibility Complex, Cryoglobulinemia, Immunoglobulin M, Rheumatoid Factor, Immunoglobulin G, Humans, Female, Genes, Dominant
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 12 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
