Infantile genetic agranulocytosis. A review with presentation of ten new cases.

作者: ROLF KOSTMANN

DOI: 10.1111/J.1651-2227.1975.TB03847.X

关键词:

摘要: A review of the literature on subject since 1956 is made in connection with a presentation ten new cases from northern Sweden. Nine these are related to main pedigree published 1956. Consanguinity between parents has been established two families. The clinical course was identical that described few additional details presented. granulocytopenia present first day life and granulocyte count subsequently rapidly decreases during week. existence diaplacental factor regarded highly probable. It assumed maturation defect precursors may be due deficiency serum factor. fact many infantile genetic agranulocytosis occur sporadically finally explained.

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