Phenotype of PLP1-related Disorder Caused by Novel Mutation: A Case Report

Mov Disord Clin Pract. 2018 Aug 2;5(5):548-550. doi: 10.1002/mdc3.12644. eCollection 2018 Sep-Oct.

Authors

Nikola Kresojević¹, Igor Petrović^{1

2}, Valerija Dobričić¹, Aleksandra Tomić^{1

2}, Vesna Branković³, Vedrana Milić Rašić^{2

3}, Marina Svetel^{1

2}, Vladimir Kostić^{1

2}

Affiliations

¹ Neurology Clinic Clinical Centre of Serbia Belgrade Serbia.
² School of Medicine University of Belgrade Belgrade Serbia.
³ Clinic for Neurology and Psychiatry for Children and Youth Belgrade Serbia.

No abstract available

Keywords: Hereditary spastic paraplegia type 2; Hypomyelination; Leukodystrophy; PLP1 gene; Pelizaeus–Merzbacher disease.

Publication types

Case Reports