CareLit · DOI-Nachweis · Aktuelle Neurologie
Complicated autosomal recessive hereditary spastic paraplegia with vertical eye movement paresis (Parinaud's syndrome): a novel phenotype caused by a new homozygous SPG7 gene mutation
DOI 10.1055/s-2006-953112
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Autor:innenT. Warnecke, A. Schwan, J.T. Epplen, P. Young
ZeitschriftAktuelle Neurologie
Ausgabe09/2006
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Aims: Hereditary spastic paraplegia (HSP) is a clinically and gentically heterogenous neurodegenerative disorder. Clinically an uncomplicated and a complicated form can be distinguished. The uncomplicated form is characterised by slow progressive spastic paraparesis and disturbation of micturition. For the complicated forms a huge number of additional symptoms have been reported. So far thirty-one different genetic…
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Zitierempfehlung
T. Warnecke, A. Schwan, J.T. Epplen, P. Young (2006) Complicated autosomal recessive hereditary spastic paraplegia with vertical eye movement paresis (Parinaud's syndrome): a novel phenotype caused by a new homozygous SPG7 gene mutation. Aktuelle Neurologie (09). https://doi.org/10.1055/s-2006-953112
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