Successful Nonmyeloablative Allogeneic Stem Cell Transplant in a Child With Emberger Syndrome and GATA2 Mutation

Author:

Rastogi Neha,Abraham Roshini S.,Chadha Ritu,Thakkar Dhwanee,Kohli Shruti,Nivargi Sagar,Prakash Yadav Satya

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference20 articles.

1. Deaf-mutism, lymphedema of the lower limbs and hematological abnormalities (acute leukemia, cytopenia) with autosomal dominant transmission [in French];Emberger;J Genet Hum,1979

2. Familial acute myeloid leukaemia with acquired Pelger-Hu€et anomaly and aneuploidy of C group;Kaur;BMJ,1972

3. Deux observations familiales d’_el_ephantiasis cong_enital avec leuc_emie aigue myeloide;Drony;Nouv Pres Fr Hemat,1983

4. Association of idiopathic lymphedema and familial acute leukemia;Attal;Apropos of a new case Presse Med,1985

5. Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new cases;Mansour;Am J Med Genet A,2010

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