Single Center Experience With Pediatric Patients With GATA2 Deficiency
GATA2 deficiency is one of the most common predisposing conditions for MDS in young individuals. It is characterized by autosomal dominant inheritance and a high rate of de novo mutations. Here we describe the clinical phenotype and hematological presentation of 10 pediatric patients with GATA2 defi...
Saved in:
Main Authors: | Galina Ovsyannikova (Author), Anna Pavlova (Author), Ekaterina Deordieva (Author), Elena Raykina (Author), Alexey Pshonkin (Author), Alexey Maschan (Author), Michael Maschan (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2022-02-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
HEMOPHAGOCYTIC SYNDROME IN EMERGENCY AND INTENSIVE PEDIATRICS
by: M.A. Maschan, et al.
Published: (2011) -
HEMOPHAGOCYTIC SYNDROME IN EMERGENCY AND INTENSIVE PEDIATRICS
by: M.A. Maschan, et al.
Published: (2011) -
GATA2 deficiency detected by newborn screening for SCID: A case report
by: Alejandra Escobar Vasco, et al.
Published: (2023) -
GATA2 mutations and overexpression in pediatric acute myeloid leukemia
by: Zhenzhen Yang, et al.
Published: (2019) -
Bone Mineral Turnover after Allogeneic Hematopoietic Stem Cell Transplantation in Children: A Single Center Cohort Study
by: Yuliya V. Skvortsova, et al.
Published: (2018)