Article citationsMore>>
Fasano, A., Nardocci, N., Emanuele, A., Zorzi, G., Bentivoglio, A. and Albanese, A. (2006) Non-DYT1 earlyonset primary torsion dystonia: Comparison with DYT1 phenotype and review of the literature. Movement Disorders, 9, 1411-1418. http://dx.doi.org/10.1002/mds.21000
has been cited by the following article:
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TITLE:
A case of mixed geno—Phenotype of generalized dystonia and strumpel disease
AUTHORS:
Vadim Belenky
KEYWORDS:
Dystonia; Strumpel Disease; DYT 1
JOURNAL NAME:
Case Reports in Clinical Medicine,
Vol.2 No.8,
November
5,
2013
ABSTRACT: Background: Strumpel disease and dystonia are inherited disorders with the clinical picture of spastic paraparesis and hyperkinesis respectively. We present a case of a patient born from parents with these diseases who developed neurologic phenomena uncharacteristic for the classical clinical picture of his parents’ disorders. Case report: Patient V., 12, born from his father with generalized dystonia and mother with Strumpel disease, has flaccid lower paraplegia along with dystonic hyperkinesis in neck and arms. Discussion: The flaccid lower paraplegia could be caused by the anterior horn lesion. This phenomenon is unclear because anterior horn lesions were not diagnosed in the proband’s parents.
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