کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1998615 1065818 2012 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Adrenoleukodystrophy in female heterozygotes: Underrecognized and undertreated
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Adrenoleukodystrophy in female heterozygotes: Underrecognized and undertreated
چکیده انگلیسی

X-linked adrenoleukodystrophy (X-ALD) is a neurodegenerative disease resulting from mutations in the gene ABCD1 and alterations in peroxisomal beta-oxidation of long chain fatty acids. As it has been frequently discussed, it manifests a wide range of phenotypes in male, with progressive myelopathy being the most common. Even though the gene is localized to the X-chromosome and a region subject to X-inactivation, female carriers still are affected significantly by this condition. It has been stated that between 20 and 50% of women who are carriers may manifest some symptoms and recent evidence has suggested the differences in disease manifestations and relative rates of progression between men and women. However there have been only limited studies specifically addressing this and to date there has been no comprehensive review discussing the different phenotypes in female carriers, as well as the differences in disease onset, progression, disability, nervous system pathology and neuroimaging patterns compared to affected males. This is of key importance as similarities and differences between genders will assist in determining how best to target therapies in all affected individuals as opportunities for treatment present themselves. As will be further addressed in this review, we need to improve our understanding of the associations of emergent neuroimaging techniques to physical disability in this population. We reviewed the clinical presentations in the carrier population, the distinct disability profile and neuroimaging findings in order to put together pieces of this neglected segment in X-ALD and give direction to further studies.


► We reviewed all the current literature on females presenting with X-ALD.
► We discuss the importance of detecting and treating carriers.
► We review the distinct clinical presentation and neuroimaging findings in this population.
► We point out the clinical trials in the carriers and outline the emergent therapies.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular Genetics and Metabolism - Volume 105, Issue 2, February 2012, Pages 180–185
نویسندگان
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