Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients.

Heterozygous germline mutations strongly predispose to leukemia, immunodeficiency, and/or lymphoedema. We describe a series of 79 patients (53 families) diagnosed since 2011, made up of all patients in France and Belgium, with a follow up of 2249 patients/years. Median age at first clinical symptoms was 18.6 years (range, 0-61 years). Severe infectious diseases (mycobacteria, fungus, and human papilloma virus) and hematologic malignancies were the most common first manifestations. The probability of remaining symptom-free was 8% at 40 years old. Among the 53 probands, 24 had missense mutations... Mehr ...

Verfasser: Donadieu, Jean
Lamant, Marie
Fieschi, Claire
de Fontbrune, Flore Sicre
Caye, Aurélie
Ouachee, Marie
Beaupain, Blandine
Bustamante, Jacinta
Poirel, Hélène
Isidor, Bertrand
Van Den Neste, Eric
Neel, Antoine
Nimubona, Stanislas
Toutain, Fabienne
Barlogis, Vincent
Schleinitz, Nicolas
Leblanc, Thierry
Rohrlich, Pierre
Suarez, Felipe
Ranta, Dana
Chahla, Wadih Abou
Bruno, Bénédicte
Terriou, Louis
Francois, Sylvie
Lioure, Bruno
Ahle, Guido
Bachelerie, Françoise
Preudhomme, Claude
Delabesse, Eric
Cave, Hélène
Bellanné-Chantelot, Christine
Pasquet, Marlène
French GATA2 study group
Dokumenttyp: Artikel
Erscheinungsdatum: 2018
Verlag/Hrsg.: Ferrata Storti Foundation
Schlagwörter: Adolescent / Adult / Belgium / Child / Preschool / France / GATA2 Deficiency / Germ-Line Mutation / Hematologic Neoplasms / Hematopoietic Stem Cell Transplantation / Humans / Infant / Newborn / Infection / Middle Aged / Mortality / Prognosis / Surveys and Questionnaires / Young Adult
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26918586
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://hdl.handle.net/2078.1/220950