Research progress in diagnosis and treatment of female heterozygotes with X-linked adrenoleukodystrophy
10.3760/cma.j.issn.2095-428X.2018.08.023
- VernacularTitle:女性杂合子X-连锁肾上腺脑白质营养不良诊断及治疗的研究进展
- Author:
Xiaole WANG
1
;
Jing PENG
Author Information
1. 中南大学湘雅医院儿科
- Keywords:
X-linked adrenoleukodystrophy;
Female heterozygotes;
ABCD1 gene
- From:
Chinese Journal of Applied Clinical Pediatrics
2018;33(8):638-640
- CountryChina
- Language:Chinese
-
Abstract:
X-linked adrenoleukodystrophy is the most common peroxisomal disorder,which belongs to single peroxidase enzyme deficiency disease.It is caused by mutations in the ABCDI gene and alterations in peroxisomal beta-oxidation of long chain fatty acid in plasma and tissues.It manifests a wide range of phenotypes in male and it has been frequently discussed,in which progressive myelopathy is the most common.For X-linked recessive inheritance,female heterozygotes are always thought to be nonpathogenic.There have been only limited studies specifically focused on the phenotype of female heterozygotes,while,these patients also need further study.This article discusses the clinical manifestations,diagnosis and treatment of female heterozygotes with X-linked adrenoleukodystrophy,to enhance people's understanding of clinical diagnosis and treatment,and provide the basis for accurate prognosis assess-ment and diagnosis.
