Genetic disorders with central nervous system white matter abnormalities: An update

Anju Shukla*, Parneet Kaur, Dhanya Lakshmi Narayanan, Michelle C. do Rosario, Rajagopal Kadavigere, Katta Mohan Girisha

*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلةReview articleمراجعة النظراء

9 اقتباسات (Scopus)

ملخص

Several genetic disorders have variable degree of central nervous system white matter abnormalities. We retrieved and reviewed 422 genetic conditions with prominent and consistent involvement of white matter from the literature. We herein describe the current definitions, classification systems, clinical spectrum, neuroimaging findings, genomics, and molecular mechanisms of these conditions. Though diagnosis for most of these disorders relies mainly on genomic tests, specifically exome sequencing, we collate several clinical and neuroimaging findings still relevant in diagnosis of clinically recognizable disorders. We also review the current understanding of pathophysiology and therapeutics of these disorders.

اللغة الأصليةEnglish
الصفحات (من إلى)119-132
عدد الصفحات14
دوريةClinical Genetics
مستوى الصوت99
رقم الإصدار1
المعرِّفات الرقمية للأشياء
حالة النشرPublished - يناير 2021
منشور خارجيًانعم

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