The Familial Histiocytoses
- 1 January 1985
- journal article
- research article
- Published by Taylor & Francis in Pediatric Pathology
- Vol. 3 (1) , 43-57
- https://doi.org/10.3109/15513818509068837
Abstract
Several rare disorders characterized by histiocytic hyperplasia are inherited as single-gene Mendelian traits. These familial forms of histiocytosis are heterogeneous and can be clearly distinguished from each other by clinical and genetic criteria. The genetic nature of these disorders can lead to familial recurrence and thus necessitates their distinction from the classical reticuloendothelioses. The clinical manifestations and modes of inheritance of the various familial histiocytoses are reviewed.Keywords
This publication has 83 references indexed in Scilit:
- A possible association between hepatitis-B antigen-negative infantile papular acrodermatitis and Epstein-Barr virus infectionThe Journal of Pediatrics, 1982
- Virus-associated hemophagocytic syndrome or maligant histiocytosis?The Journal of Pediatrics, 1982
- X-Linked Lymphoproliferative Syndrome Registry reportThe Journal of Pediatrics, 1980
- Combined immunodeficiency presenting as the Letterer-Siwe syndromeThe Journal of Pediatrics, 1974
- Combined immunodeficiency and reticuloendotheliosis with eosinophiliaThe Journal of Pediatrics, 1974
- Hepatosplenomegaly, pancytopenia, and feverThe Journal of Pediatrics, 1973
- Reticuloendothelial failure in familial erythrophagocytic lymphohistiocytosisThe Journal of Pediatrics, 1972
- Blood and bone-marrow findings incongenital rubellaThe Journal of Pediatrics, 1967
- The Children's Hospital Medical Center, Boston, Mass.The Journal of Pediatrics, 1962
- Familial Letterer-Siwe disease: Report of a caseThe Journal of Pediatrics, 1962