Brainstem dominant form of X-linked adrenoleukodystrophy with a novel ABCD1 missense variant: A case report and literature review.

IF 1.5 4区 医学 Q4 GENETICS & HEREDITY
Yulai Kang, Lu Guo, Zhuo Min, Lei Zhang, Lili Zhang, Chunhua Tang
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引用次数: 0

Abstract

Background: X-linked adrenoleukodystrophy (X-ALD) is the most common peroxisomal disorder attributed to ABCD1 mutations. Case reports with predominant brainstem involvement are rare.

Case presentation: In this study, we reported a plateau male worker of X-ALD characterized by progressive weakness accompanied by gait instability, mild nystagmus, and constipation. After 2 years of onset, a brain Magnetic Resonance Image (MRI) scan showed no abnormality but genetic analysis revealed a heterozygous mutation (c.1534G>A) in the ABCD1 gene. After 7 years of onset, although the patient was given aggressive dietary and symptomatic treatment in the course of the disease, a brain MRI scan showed predominantly brainstem damage, but serum concentrations of very long-chain fatty acids were normal, and he had been bedridden for almost 2 years with severe bladder dysfunction, forcing him to undergo cystostomy. The patient was discharged with improved urinary retention and renal function.

Conclusions: We reported an X-ALD patient with a novel ABCD1 variation characterized by brainstem damage and retrospectively summarized the clinical manifestation, MRI features, and genetic features of X-ALD patients with brainstem damage.

伴有新型 ABCD1 错义变异的 X 连锁肾上腺白质营养不良症脑干显性型:病例报告和文献综述
背景:X连锁肾上腺白质营养不良症(X-ALD)是因ABCD1基因突变引起的最常见的过氧化物酶体疾病。以脑干受累为主的病例报告非常罕见:在本研究中,我们报告了一名高原男性 X-ALD 患者,其特征是进行性乏力,伴有步态不稳、轻度眼球震颤和便秘。发病 2 年后,脑部磁共振成像(MRI)扫描未发现异常,但基因分析显示 ABCD1 基因存在杂合突变(c.1534G>A)。发病 7 年后,虽然患者在病程中接受了积极的饮食治疗和对症治疗,但脑磁共振成像扫描显示主要是脑干受损,但血清中长链脂肪酸的浓度正常,患者卧床近 2 年,伴有严重的膀胱功能障碍,不得不接受膀胱造口术。患者出院后,尿潴留和肾功能均有所改善:我们报告了一名以脑干损害为特征的新型ABCD1变异X-ALD患者,并回顾性总结了脑干损害X-ALD患者的临床表现、磁共振成像特征和遗传特征。
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来源期刊
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
4.20
自引率
0.00%
发文量
241
审稿时长
14 weeks
期刊介绍: Molecular Genetics & Genomic Medicine is a peer-reviewed journal for rapid dissemination of quality research related to the dynamically developing areas of human, molecular and medical genetics. The journal publishes original research articles covering findings in phenotypic, molecular, biological, and genomic aspects of genomic variation, inherited disorders and birth defects. The broad publishing spectrum of Molecular Genetics & Genomic Medicine includes rare and common disorders from diagnosis to treatment. Examples of appropriate articles include reports of novel disease genes, functional studies of genetic variants, in-depth genotype-phenotype studies, genomic analysis of inherited disorders, molecular diagnostic methods, medical bioinformatics, ethical, legal, and social implications (ELSI), and approaches to clinical diagnosis. Molecular Genetics & Genomic Medicine provides a scientific home for next generation sequencing studies of rare and common disorders, which will make research in this fascinating area easily and rapidly accessible to the scientific community. This will serve as the basis for translating next generation sequencing studies into individualized diagnostics and therapeutics, for day-to-day medical care. Molecular Genetics & Genomic Medicine publishes original research articles, reviews, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented.
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