Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia

Severe congenital neutropenia (SCN) is a rare disease that involves a heterogeneous group of hereditary diseases. Mutations in the HAX1 gene can cause an autosomal recessive form of SCN-characterized low blood neutrophil count from birth, increased susceptibility to recurrent and life-threatening in...

Full description

Saved in:
Bibliographic Details
Main Authors: Tham Thi Tran, Quang Van Vu, Taizo Wada, Akihiro Yachie, Huong Le Thi Minh, Sang Ngoc Nguyen
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Case Reports in Pediatrics
Online Access:http://dx.doi.org/10.1155/2018/2798621
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850214957322338304
author Tham Thi Tran
Quang Van Vu
Taizo Wada
Akihiro Yachie
Huong Le Thi Minh
Sang Ngoc Nguyen
author_facet Tham Thi Tran
Quang Van Vu
Taizo Wada
Akihiro Yachie
Huong Le Thi Minh
Sang Ngoc Nguyen
author_sort Tham Thi Tran
collection DOAJ
description Severe congenital neutropenia (SCN) is a rare disease that involves a heterogeneous group of hereditary diseases. Mutations in the HAX1 gene can cause an autosomal recessive form of SCN-characterized low blood neutrophil count from birth, increased susceptibility to recurrent and life-threatening infections, and preleukemia predisposition. A 7-year-old boy was admitted due to life-threatening infections, mental retardation, and severe neutropenia. He had early-onset bacterial infections, and his serial complete blood count showed persistent severe neutropenia. One older sister and one older brother of the patient died at the age of 6 months and 5 months, respectively, because of severe infection. Bone marrow analysis revealed a maturation arrest at the promyelocyte/myelocyte stage with few mature neutrophils. In direct DNA sequencing analysis, we found a novel homozygous frameshift mutation (c.423_424insG, p.Gly143fs) in the HAX1 gene, confirming the diagnosis of SCN. The patient was successfully treated with granulocyte colony-stimulating factor (G-CSF) and antibiotics. A child with early-onset recurrent infections and neutropenia should be considered to be affected with SCN. Genetic analysis is useful to confirm diagnosis. Timely diagnosis and suitable treatment with G-CSF and antibiotics are important to prevent further complication.
format Article
id doaj-art-82dbe9ed98fb4cb098389f856d8a6dd4
institution OA Journals
issn 2090-6803
2090-6811
language English
publishDate 2018-01-01
publisher Wiley
record_format Article
series Case Reports in Pediatrics
spelling doaj-art-82dbe9ed98fb4cb098389f856d8a6dd42025-08-20T02:08:46ZengWileyCase Reports in Pediatrics2090-68032090-68112018-01-01201810.1155/2018/27986212798621Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital NeutropeniaTham Thi Tran0Quang Van Vu1Taizo Wada2Akihiro Yachie3Huong Le Thi Minh4Sang Ngoc Nguyen5Department of Pediatrics, Haiphong University of Medicine and Pharmacy, Haiphong, VietnamDepartment of Pediatrics, Haiphong University of Medicine and Pharmacy, Haiphong, VietnamDepartment of Pediatrics, Institute of Medical, Pharmaceutical and Health Science, Kanazawa University, Kanazawa, JapanDepartment of Pediatrics, Institute of Medical, Pharmaceutical and Health Science, Kanazawa University, Kanazawa, JapanNational Hospital of Pediatrics, Hanoi, VietnamDepartment of Pediatrics, Haiphong University of Medicine and Pharmacy, Haiphong, VietnamSevere congenital neutropenia (SCN) is a rare disease that involves a heterogeneous group of hereditary diseases. Mutations in the HAX1 gene can cause an autosomal recessive form of SCN-characterized low blood neutrophil count from birth, increased susceptibility to recurrent and life-threatening infections, and preleukemia predisposition. A 7-year-old boy was admitted due to life-threatening infections, mental retardation, and severe neutropenia. He had early-onset bacterial infections, and his serial complete blood count showed persistent severe neutropenia. One older sister and one older brother of the patient died at the age of 6 months and 5 months, respectively, because of severe infection. Bone marrow analysis revealed a maturation arrest at the promyelocyte/myelocyte stage with few mature neutrophils. In direct DNA sequencing analysis, we found a novel homozygous frameshift mutation (c.423_424insG, p.Gly143fs) in the HAX1 gene, confirming the diagnosis of SCN. The patient was successfully treated with granulocyte colony-stimulating factor (G-CSF) and antibiotics. A child with early-onset recurrent infections and neutropenia should be considered to be affected with SCN. Genetic analysis is useful to confirm diagnosis. Timely diagnosis and suitable treatment with G-CSF and antibiotics are important to prevent further complication.http://dx.doi.org/10.1155/2018/2798621
spellingShingle Tham Thi Tran
Quang Van Vu
Taizo Wada
Akihiro Yachie
Huong Le Thi Minh
Sang Ngoc Nguyen
Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
Case Reports in Pediatrics
title Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
title_full Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
title_fullStr Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
title_full_unstemmed Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
title_short Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia
title_sort novel hax1 gene mutation in a vietnamese boy with severe congenital neutropenia
url http://dx.doi.org/10.1155/2018/2798621
work_keys_str_mv AT thamthitran novelhax1genemutationinavietnameseboywithseverecongenitalneutropenia
AT quangvanvu novelhax1genemutationinavietnameseboywithseverecongenitalneutropenia
AT taizowada novelhax1genemutationinavietnameseboywithseverecongenitalneutropenia
AT akihiroyachie novelhax1genemutationinavietnameseboywithseverecongenitalneutropenia
AT huonglethiminh novelhax1genemutationinavietnameseboywithseverecongenitalneutropenia
AT sangngocnguyen novelhax1genemutationinavietnameseboywithseverecongenitalneutropenia