Association of acute leukemia and autoimmune polyendocrine syndrome in two kindreds.

Adult; Family Health; Fathers; Female; HLA-A1 Antigen/metabolism; Humans; Male; Nuclear Family; Pedigree; Polyendocrinopathies, Autoimmune/complications/genetics/therapy; Precursor Cell Lymphoblastic Leukemia-Lymphoma/complications/genetics/therapy

Disciplines :

Hematology
Endocrinology, metabolism & nutrition

Author, co-author :

Willems, Evelyne ; Université de Liège - ULiège > Hématologie clinique

Valdes Socin, Hernan Gonzalo ; Université de Liège - ULiège > Endocrinologie clinique

Betea, Daniela ; Centre Hospitalier Universitaire de Liège - CHU > Endocrinologie clinique

Beckers, Albert ; Université de Liège - ULiège > Département des sciences cliniques > Endocrinologie

Beguin, Yves ; Université de Liège - ULiège > Hématologie clinique

Language :

English

Title :

Association of acute leukemia and autoimmune polyendocrine syndrome in two kindreds.

Publication date :

September 2003

Journal title :

Leukemia

ISSN :

0887-6924

eISSN :

1476-5551

Publisher :

Nature Publishing Group, London, United Kingdom

Volume :

Issue :

Pages :

1912-1914

Peer reviewed :

Peer Reviewed verified by ORBi

Available on ORBi :

since 16 March 2009

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Bibliography

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Tomer Y, Greenberg DA, Concepcion E, Ban Y, Davies TF. Thyroglobulin is a specific gene for the familial autoimmune thyroid diseases. J Endocrinol Metab 2001; 87: 404-407.
Horwitz M. The genetics of familial leukemia. Leukemia 1997; 11: 1347-1359.
Moskowitz C, Dutcher JP, Wiernik PH. Association of thyroid disease with acute leukemia. Am J Hematol 1992; 39: 102-107.
De Rosa G, Della S, Corsello SM, Cecchini L, Calla C. Autoimmune polyglandular syndrome, primary empty sella, and acute lymphocytic leukaemia. Clin Endocrinol 1987; 27: 535-543.
Ergas D, Tsimanis A, Shtalrid M, Duskin C, Berrebi A. T-γ large granular lymphocyte leukemia associated with amegakaryocytic thrombocytopenic purpura, Sjögren's syndrome, and polyglandular autoimmune syndrome type II, with subsequent development of pure red cell aplasia. Am J Hematol 2002; 69: 132-134.