-transparent.png){kind=logo}
It is reported on the common appearance of a hyperlipoproteinaemia type II after Fredrickson and of a selective insufficiency of IgM in a family. The two generations of a family which have been observed since three years show these disturbances in a 42-year-old patient and all his four children. The diminution and the lack of a stimulation of B-cells under antihuman-IgM in the transformation test of lymphocytes refer to an isolated disturbance of the IgM-synthesis. Cellular immune reactions and haematologically cytological findings were normal. A connection between the lack of IgM and hypercholesterolaemia is not excluded, since experimental investigations of Alderson and Green show an influence of cholesterol on the function of the lymphocyte membrane. The necessity of systematic investigations on patients with immune defects and hyperlipoproteinaemias is emphasized for the exclusion of an accidental coincidence.
H Storch, and
B Kuklinski, and
H Schwenke
September 1979,
Atherosclerosis,
H Storch, and
B Kuklinski, and
H Schwenke
April 1971,
Clinical science,
H Storch, and
B Kuklinski, and
H Schwenke
September 1976,
Metabolism: clinical and experimental,
H Storch, and
B Kuklinski, and
H Schwenke
February 1976,
Pediatrics,
H Storch, and
B Kuklinski, and
H Schwenke
July 1974,
American journal of diseases of children (1960),
H Storch, and
B Kuklinski, and
H Schwenke
January 1973,
Nutrition and metabolism,
H Storch, and
B Kuklinski, and
H Schwenke
August 1969,
Minerva pediatrica,
H Storch, and
B Kuklinski, and
H Schwenke
January 1968,
University of Michigan Medical Center journal,
H Storch, and
B Kuklinski, and
H Schwenke
June 1968,
Arthritis and rheumatism,
H Storch, and
B Kuklinski, and
H Schwenke
May 1992,
Klinische Monatsblatter fur Augenheilkunde,
