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

International audience ; 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 prob... 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: Artikel
Erscheinungsdatum: 2018
Verlag/Hrsg.: HAL CCSD
Schlagwörter: [SDV]Life Sciences [q-bio]
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26494136
Datenquelle: BASE; Originalkatalog
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Link(s) : https://hal.univ-lille.fr/hal-04318378