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

Heterozygous germline GATA2 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 mut... Mehr ...

Verfasser: Donadieu, Jean
Lamant, Marie
Fieschi, Claire
Sicre De Fontbrune, Flore
Caye, Aurelie
Ouachee, Marie
Beaupain, Blandine
Bustamante, Jacinta
Poirel Helene, A
Isidor, Bertrand
Van Den Neste, Eric
Neel, Antoine
Nimubona, Stanislas
Toutain, Fabienne
Barlogis, Vincent
Schleinitz, Nicolas
Leblanc, Thierry
Rohrlich, Pierre-Simon
Suarez, Felipe
Ranta, Dana
Abou Chahla, Wadih
Bruno, Benedicte
Terriou, Louis
Francois, Sylvie
Lioure, Bruno
Ahle, Guido
Bachelerie, Francoise
Preudhomme, Claude
Delabesse, Eric
Cave, Helene
Bellanne-Chantelot, Christine
Pasquet, Marlene
Dokumenttyp: article dans une revue scientifique
Erscheinungsdatum: 2019
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-27305189
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://hdl.handle.net/20.500.12210/4527