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

European Journal of Pediatrics

Volumn 171, Issue 8, 2012, Pages 1273-1276

  Ishida, Hiroyuki ^a   Imai, Kosuke ^b   Honma, Kenichi ^c   Tamura, Shin Ichi ^a   Imamura, Toshihiko ^d   Ito, Masafumi ^e   Nonoyama, Shigeaki ^c  

^a MATSUSHITA MEMORIAL HOSPITAL   (Japan)

^b TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^c NATIONAL DEFENSE MEDICAL COLLEGE   (Japan)

^d KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^e JAPANESE RED CROSS NAGOYA FIRST HOSPITAL   (Japan)

Author keywords

B and NK cell lymphopenia; Emberger syndrome; Immunodeficiency; Monocytopenia; MonoMAC; Myelodysplasia

Indexed keywords

COMPLEMENTARY DNA; TRANSCRIPTION FACTOR GATA 2;

ADOLESCENT; ARTICLE; AUTOIMMUNE DISEASE; CASE REPORT; FEMALE; FEVER; FLOW CYTOMETRY; GENE MUTATION; GENE SEQUENCE; HERPES ZOSTER; HUMAN; LUNG INFECTION; LYMPHEDEMA; LYMPHOCYTOPENIA; MONOCYTE; MONOCYTOPENIA; MYELODYSPLASTIC SYNDROME; NATURAL KILLER CELL; NEUTROPENIA; PANNICULITIS; PHENOTYPE; PRIORITY JOURNAL; SALMONELLOSIS; T LYMPHOCYTE; VARICELLA ZOSTER VIRUS;

FEMALE; GATA2 TRANSCRIPTION FACTOR; GENETIC MARKERS; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; LYMPHEDEMA; MUTATION, MISSENSE; MYELODYSPLASTIC SYNDROMES; PHENOTYPE; SYNDROME; YOUNG ADULT;

EID: 84866039522     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/s00431-012-1715-7     Document Type: Article

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