-transparent.png){kind=logo}
This report concerns a young woman, whose stained blood films revealed a hypochromic and microcytic red cell morphology. It could be shown by haemoglobin analysis that this atypical blood film was due to a double heterozygote disorder of haemoglobin D (Hb D) and beta-thalassaemia. The thalassaemia trait was inherited from her father and the Hb D from her mother. This is the first observation of this rare disorder in a German family. Comparable cases reported in the literature are mentioned.
Related Publications
H Piechowiak, and
M Krause, and
E Kohne
August 1984,
The Indian journal of medical research,
H Piechowiak, and
M Krause, and
E Kohne
January 1980,
Acta haematologica,
H Piechowiak, and
M Krause, and
E Kohne
January 1975,
Acta haematologica,
H Piechowiak, and
M Krause, and
E Kohne
July 1968,
Journal of clinical pathology,
H Piechowiak, and
M Krause, and
E Kohne
June 1965,
British medical journal,
H Piechowiak, and
M Krause, and
E Kohne
January 1979,
Acta medica Austriaca,
H Piechowiak, and
M Krause, and
E Kohne
March 1969,
British journal of haematology,
H Piechowiak, and
M Krause, and
E Kohne
January 1978,
Acta haematologica,
H Piechowiak, and
M Krause, and
E Kohne
January 1999,
European journal of human genetics : EJHG,
H Piechowiak, and
M Krause, and
E Kohne
November 1968,
Nature,
