Digenic mutations in severe congenital neutropenia

被引:42
作者
Germeshausen, Manuela [1 ]
Zeidler, Cornelia
Stuhrmann, Manfred [2 ]
Lanciotti, Marina [3 ]
Ballmaier, Matthias
Welte, Karl
机构
[1] Hannover Med Sch, Dept Pediat Hematol & Oncol Mol Hematopoiesis, D-30625 Hannover, Germany
[2] Hannover Med Sch, Inst Human Genet, D-3000 Hannover, Germany
[3] Giannina Gaslini Inst, Dept Pediat Hematol & Oncol, Genoa, Italy
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2010年 / 95卷 / 07期
关键词
ELANE; congenital neutropenia; HAX1; myelopoiesis; ELASTASE; GENE; DEFICIENCY; PHENOTYPE; DISEASE; ELA2;
D O I
10.3324/haematol.2009.017665
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Severe congenital neutropenia a clinically and genetically heterogeneous disorder. Mutations in different genes have been described as causative for severe neutropenia, e.g. ELANE, HAX1 and G6PC3. Although congenital neutropenia is considered to be a group of monogenic disorders, the phenotypic heterogeneity even within the yet defined genetic subtypes points to additional genetic and/or epigenetic influences on the disease phenotype. We describe congenital neutropenia patients with mutations in two candidate genes each, including 6 novel mutations. Two of them had a heterozygous ELANE mutation combined with a homozygous mutation in G6PC3 or HAX1, respectively. The other 2 patients combined homozygous or compound heterozygous mutations in G6PC3 or HAX1 with a heterozygous mutation in the respective other gene. Our results suggest that digenicity may underlie this disorder of myelopoiesis at least in some congenital neutropenia patients.
引用
收藏
页码:1207 / 1210
页数:4
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