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Clinical and molecular characterization of autosomal recessive forms of hereditary spastic paraplegia with cognitive deficits

J Doeringer, B Winner, G Uyanik, A Oelmez, U Bogdahn, U Hehr, J Winkler · Aktuelle Neurologie · Ausgabe 09/2007

DOI 10.1055/s-2007-987782

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Autor:innenJ Doeringer, B Winner, G Uyanik, A Oelmez, U Bogdahn, U Hehr, J Winkler
ZeitschriftAktuelle Neurologie
Ausgabe09/2007
Jahrgang / SeitenNicht angegeben

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Aims: Hereditary spastic paraplegias (HSPs) comprise a clinically and genetically heterogeneous group of neurodegenerative disorders, resulting in progressive spasticity of the lower limbs. In contrast to “pure HSP“, additional clinical features are present in patients with complicated HSP. Based on the mode of inheritance (autosomal recessive, autosomal dominant and X-linked) and the linkage data, to date, 36 disti…

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J Doeringer, B Winner, G Uyanik, A Oelmez, U Bogdahn, U Hehr, J Winkler (2007) Clinical and molecular characterization of autosomal recessive forms of hereditary spastic paraplegia with cognitive deficits. Aktuelle Neurologie (09). https://doi.org/10.1055/s-2007-987782

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