先天性中性粒细胞减少
中性粒细胞减少症
突变
复合杂合度
表型
遗传异质性
遗传学
免疫学
生物
基因
化疗
作者
Manuela Germeshausen,Cornelia Zeidler,Manfred Stuhrmann,Marina Lanciotti,Matthias Ballmaier,Karl Welte
出处
期刊:Haematologica
[Ferrata Storti Foundation]
日期:2010-03-10
卷期号:95 (7): 1207-1210
被引量:57
标识
DOI:10.3324/haematol.2009.017665
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.
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