A rare case of adult-onset vanishing white matter leukoencephalopathy with movement disorder, expressing homozygous EIF2B3 and PRKN pathogenic variants

  1. Bashar Kamal Ali Douden
  2. Yazan Mohammad Abdullah Abufara
  3. Mahmood Fayez Ali Aldrabeeh
  4. Naela Ramadan Mohammad Tell
  5. Ismail Abudaya
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  1. Version published to 10.1186/s12883-024-04018-y
  2. Version published to 10.21203/rs.3.rs-5241534/v1 on Research Square