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Research progress in diagnosis and treatment of female heterozygotes with X-linked adrenoleukodystrophy / 中华实用儿科临床杂志
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-696463
Responsible library: WPRO
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.

Full text: Available Database: WPRIM (Western Pacific) Type of study: Diagnostic study Language: Chinese Journal: Chinese Journal of Applied Clinical Pediatrics Year: 2018 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Type of study: Diagnostic study Language: Chinese Journal: Chinese Journal of Applied Clinical Pediatrics Year: 2018 Document type: Article
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