GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia.

Ishida, Hiroyuki

GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia. [electronic resource] - European journal of pediatrics Aug 2012 - 1273-6 p. digital

Publication Type: Case Reports; Journal Article

1432-1076

10.1007/s00431-012-1715-7 doi


Female
GATA2 Transcription Factor--genetics
Genetic Markers
Humans
Immunologic Deficiency Syndromes--diagnosis
Lymphedema--diagnosis
Mutation, Missense
Myelodysplastic Syndromes--diagnosis
Phenotype
Syndrome
Young Adult