4.5 Article

Typical and atypical phenotype and neuroimaging of X-linked adrenoleukodystrophy in a Chinese cohort

期刊

NEUROLOGICAL SCIENCES
卷 43, 期 5, 页码 3255-3263

出版社

SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s10072-021-05859-y

关键词

X-linked adrenoleukodystrophy; Phenotype; Genotype; Adrenomyeloneuropathy; Spinocerebellar variant

资金

  1. National Key Research and Development Program of China [2020YFA0804500]
  2. CAMS Innovation Fund for Medical Sciences (CIFMS) [2020-I2M-CT-B-010, 2016-I2M-1-004]
  3. National Natural Science Foundation of China [81550021, 30470618]

向作者/读者索取更多资源

This study describes the typical and atypical clinical and neuroimaging features of ALD in Chinese patients, which can contribute to early diagnosis and intervention for improved prognosis.
Objective The objective of this study is to describe the typical and atypical clinical and neuroimaging features of ALD in Chinese patients, which will help early diagnosis and intervention to improve prognosis of ALD. Methods Forty-one patients in the Leukoencephalopathy Clinic of Neurology Department, Peking Union Medical College Hospital were enrolled. Detailed clinical manifestations and MRI features were analyzed. The relationship between phenotype and genotype as well as biochemical analysis was observed. Results The patients were classified according to phenotype and onset age, including 14 childhood cerebral ALD (CCALD), 8 adolescent cerebral ALD (adoCALD), 3 adult cerebral ALD (ACALD), 14 adrenomyeloneuropathy (AMN), and 2 ALD in women. AMN was the main presentation in adults. Visual impairment was usual onset symptom in CCALD and cognitive decline and psychiatric symptoms were found in adoCALD and ACALD. Typical MRI feature of CALD was symmetrical peri-ventricular butterfly wings like lesions in frontal and/or occipital lobe with peripheral DWI hyperintensities and Gd enhancement. Corpus callosum and internal capsule were always involved. Unilateral lesions were also possible. Cerebral AMN presented with centrum semiovale diffuse involvement. Spinocerebellar variant was a special subtype of AMN with obvious cerebellar and brainstem lesions. No relationships between phenotype and genotype as well as biochemical VLCFAs analysis were found. Conclusions We emphasize that corpus callosum and internal capsule are always involved in ALD. A unilateral lesion is also possible. Neuroimaging of cerebral AMN is different from typical CALD with more centrum semiovale involvement. We support spinocerebellar variant was a rare subtype of AMN.

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