An unusual case with genetic transition in a rehabilitation clinic: Troyer syndrome-Reference-Cited by-同舟云学术

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An unusual case with genetic transition in a rehabilitation clinic: Troyer syndrome

Published:2021-05-25 Issue:2 Volume:67 Page:264-265
ISSN:2587-1250
Container-title:Turkish Journal of Physical Medicine and Rehabilitation
language:en
Short-container-title:Turk J Phys Med Rehab

Author:

Gürçay Eda^ORCID,Büşra Ayçiçek Hilal^ORCID,Zeliha Karaahmet Özgür^ORCID,Korkmaz Nurdan^ORCID,Yaşar Evren^ORCID

Publisher

Baycinar Tibbi Yayincilik

Subject

Rehabilitation,Physical Therapy, Sports Therapy and Rehabilitation

Link

http://www.ftrdergisi.com/uploads/pdf/pdf_4296.pdf

Reference4 articles.

1. Fink JK. Hereditary spastic paraplegia overview. Gene Reviews. 2000. Last Update: 2014. Available at: https://www. ncbi.nlm. nih.gov/books/NBK1509/.

2. Manzini MC, Rajab A, Maynard TM, Mochida GH, Tan WH, Nasir R, et al. Developmental and degenerative features in a complicated spastic paraplegia. Ann Neurol 2010;67:516-25.

3. Proukakis C, Cross H, Patel H, Patton MA, Valentine A, Crosby AH. Troyer syndrome revisited. A clinical and radiological study of a complicated hereditary spastic paraplegia. J Neurol 2004;251:1105-10.

4. Neuhäuser G, Wiffler C, Opitz JM. Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or "new" syndrome. Clin Genet 1976;9:315-23.

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