“…This patient has a high titre of thyroid antibodies, very low B,, values and a Schilling test of 7 yo absorption of BIZ. Her anemia was treated in a paper by Larsson (7). I t seems almost certain that this is an instance of myeloma even though the high titre of thyroid antibodies is an unusual finding.…”
Section: The Following Three Patients Have Had Slowly Developing Myelmentioning
“…This patient has a high titre of thyroid antibodies, very low B,, values and a Schilling test of 7 yo absorption of BIZ. Her anemia was treated in a paper by Larsson (7). I t seems almost certain that this is an instance of myeloma even though the high titre of thyroid antibodies is an unusual finding.…”
Section: The Following Three Patients Have Had Slowly Developing Myelmentioning
“…Myeloma and asyniptomatic M-component occurring in !he .Tame family has been reported in couples of siblings in three families (13,23). (The asymptomatic M-components belonged to the types yG (13,23) and yM (23).)…”
Section: Investigations Of Further Relatives Of the 64 Individualsmentioning
confidence: 97%
“…Myeloma and asyniptomatic M-component occurring in !he .Tame family has been reported in couples of siblings in three families (13,23). (The asymptomatic M-components belonged to the types yG (13,23) and yM (23).) The clue to the findings of Spengler et al (23) was a systematic investigation of 110 relatives of 22 individuals with M-components of different kinds (myeloma 14, macroglobulinaemia Waldenstrorn six and asymptomatic M-component two).…”
Section: Investigations Of Further Relatives Of the 64 Individualsmentioning
Two families with multiple occurrence of M‐components are reported. In one family a mother and her son had M‐components. The latter had myeloma with γGK and γAK M‐components, the mother had a probable myeloma with γGK M‐component. Investigation of eight close relatives revealed no further M‐component. In another family three siblings had M‐components. A sister had a myeloma with exclusively light chain (Bence‐Jones) myeloma protein while two brothers had asymtomatic γGK M‐components and Bence‐Jones proteinuria respectively (the Bence‐Jones proteins in both cases were of type lambda). The significance of genetic factors in these familial cases is discussed in relation to the known figures of the frequency of M‐components and myeloma in Swedish populations.
“…She has pernicious anemia and this problem has been treated by S.O. Larsson in a recent publication (9). We have followed her y-globulin values, and her general status since 1956 has been quite unchanged (nearly 6 years).…”
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