Hereditary Nephritis Associated with May-Hegglin Anomaly
- 1 January 1981
- journal article
- research article
- Published by S. Karger AG in Nephron
- Vol. 29 (1-2), 59-62
- https://doi.org/10.1159/000182240
Abstract
Hereditary nephritis associated with hematologic abnormalities seems to be an exceptional occurrence. We have observed a family in which nephritis was combined with May-Hegglin anomaly. A girl and her father suffered from proteinuria; a paternal uncle received a kidney graft; a paternal grand aunt died on periodic hemodialysis. The girl, the father and the uncle presented macrothrombocytopenia (40–100 × 109/l, size 4–8 µm) with prolonged bleeding time (which precluded renal biopsy) and cytoplasmic inclusions in neutrophils (Döhle bodies). These hematologic abnormalities characterize the May-Hegglin anomaly. This kind of association has not been reported on so far.Keywords
This publication has 10 references indexed in Scilit:
- Megathrombocytopenia Associated with Glomerulonephritis, Deafness and Aortic Cystic MedianecrosisScandinavian Journal of Haematology, 1978
- Megakaryocyte Polyploidization in May-Hegglin AnomalyActa Haematologica, 1978
- Thrombocytopenia, macrothrombocytopathia, nephritis and deafnessAmerican Journal Of Medicine, 1976
- Hereditary nephritis, deafness and abnormal thrombopoiesisAmerican Journal Of Medicine, 1976
- Hereditary Thrombocytopenia, Deafness, and Renal DiseaseAnnals of Internal Medicine, 1975
- Platelet factor 3 in normal subjects and patients with renal failureJournal of Clinical Investigation, 1968
- Platelet Survival in the May-Hegglin Anomaly*British Journal of Haematology, 1966
- Platelet Sequestration in Man. I. Methods*Journal of Clinical Investigation, 1964
- The aggregation of blood plateletsThe Journal of Physiology, 1963
- Leukocytic Inclusions—Döhle Bodies—Associated with Platelet Abnormality (The May-Hegglin Anomaly)Blood, 1962