Mean corpuscular hemoglobin is increased in Martin-Bell syndrome |
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Authors: | U. Langenbeck J. Schmidtke Iris Bartels I. Hansmann H. Knüppel |
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Affiliation: | (1) Institute of Human Genetics, University of Göttingen, D-3400 Gottingen, Germany;(2) Rotenburger Anstalten der Inneren Mission, Rotenburg/Wümme, Germany |
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Abstract: | Summary Studying the blood picture of 11 patients with Martin-Bell syndrome, we found the erythrocytes relatively hyperchromic when compared to the data from 171 matched controls living in the same institution. Because mean corpuscular hemoglobin is increased also in patients with folic acid deficiency states, we feel that our data provide further evidence that Martin-Bell syndrome is an inherited disease of folate metabolism.The data were first presented at the 18th Meeting of the Gesellschaft für Anthropologie und Humangenetik, Münster/Westf., October 5–8, 1983 |
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